“素养为本”的化学课堂教学*——以“原子晶体”为例

基于“素养为本”视角,以“原子晶体”的教学为例,对教学主题内容、教学现状及学情进行分析;以发展学生化学学科核心素养为主旨确定教学目标;以“微粒-微粒间的相互作用-物质的聚集状态-物质性质”的认识思路为主线,以“模型认知,建构概念-证据推理,归纳性质-微观探析,探究结构-科学史实,揭示价值”的任务型教学流程,达到落实并发展学生化学学科核心素养的目的。     

基于学科理解的“醛的结构与性质探究”教学设计与实施

学科理解是教师教学的坚实基础,教学设计环节首先进行学科理解研究,通过阐释“如何基于极性多重键认识羰基化合物的结构与性质？”本原性问题,对主题学科大概念“有机物构性关系”进行本原性、结构化地理解。从教学目标、教学思路、教学实施过程阐述“醛的结构与性质探究”一课的教学。课后阶段进行学生访谈及分析、专家评价和教师反思总结。系统地呈现基于学科理解的素养为本的课堂教学研究。     

跨学科项目教学案例*——魔力沙

以魔术表演用的沙子为素材,开发了适用于高中选修课程“发展中的化学学科”的具有跨学科性的项目教学案例,该项目弱化理论分析环节后也可以用于初中科学实践活动课程。项目引导学生在更宽广的学科背景下认识物质及其变化的规律,帮助学生拓展视野和思路,综合运用化学、物理等学科的知识分析解决有关问题,发展“宏观辨识与微观探析”“科学探究与创新意识”“科学态度与社会责任”等化学学科核心素养。     

促进知识素养化的教学——以“硝酸的性质”为例

以“铜制品抛光液”为情境素材,设计一系列的情境问题,旨在探究浓度、温度、酸度等因素对硝酸强氧化性的影响、硝酸的不稳定性及硝酸的贮输等核心内容。开展以化学实验为主的多种探究活动,学生在问题解决和探究过程中结构化“硝酸的性质”知识,利用结构化的知识评价铜制品抛光液的优缺点,并对此种抛光液提出合理的改进方案,促使知识素养化,落实学生的化学学科核心素养。     

促进学生化学学科核心素养发展的“铁盐和亚铁盐”的单元教学

设计了“铁盐和亚铁盐”的单元教学,以“探究硫酸亚铁的性质”和“线路板腐蚀液的研究”为核心任务,把铁盐与亚铁盐的性质、Fe²⁺和Fe³⁺的相互转化等核心知识贯穿其中,建立从物质类别、元素价态视角研究物质性质及转化的思路方法,促进多维度化学学科核心素养的融合发展。经过多轮次教学改进,结合教学实践过程及其教学效果抽提出“注重应用无机物的认识模型,重点把握研究物质性质的角度和思路”“抓住典型活动,培养学生的关键能力”“设计开放性任务,通过有效的师生对话进行诊断,外显问题解决思路”等教学策略。     

基于真实情境的初中化学微项目教学实践与反思*——以“溶液的形成”为例

以“溶液的形成”为例进行微项目教学实践,选择学生熟悉的护手霜为主题情境,巧妙设计了“原料分散”“微观探秘”“辨识活动”“对比实验”“感知乳化”等系列微项目活动,通过情境不断地设置认知冲突,引导学生反思、修正并最终形成更完善的概念,在环环相扣的探究活动中使学生自主建构结构化的知识。通过制作“护手霜”将“溶解”和“乳化”串联,感知溶液,感受乳化,感悟人与自然、社会的和谐、可持续发展。     

基于交叉优势特色学科的大学化学创新实验教学体系构建与实践*

以大学化学与农林优势学科交叉融合为教学改革任务,构建“基础+模块”的大学化学实验创新教学体系,分别开展“项目式”教学、“科教融合”教学、“产学研”教学、“混合式”教学、“虚实结合”教学等五位一体的实验教学实践,并建立化学创新实验课程评价新体系。本化学创新实验教学体系改革明显提高了学生的实践动手能力与综合素质,为深入开展化学基础学科与农林优势学科交叉融合教学奠定一定基础。     

促进学生认识发展的学科教学认识的构建——以“原电池”为例

阐释了学科教学认识和促进学生认识发展教学的基本内涵,在此基础上结合化学学科和“原电池”的内容特点,从有关“原电池”的学科知识、课程知识、学生理解的知识、教学策略及表征的知识等4个方面,论述了“原电池”主题的学科教学认识的构建。     

课程思政视角下化学思维型课堂的建构*——以“乙醇”的教学为例

通过以真实问题为情境,以化学知识结构化与化学核心观念为基础,以问题的探究为路径,以乙醇教学为例,建构了课程思政视角下的化学思维型课堂即“两思课堂”的基本教学模型,探索了“两思课堂”的评价方法与内容。通过分析学生表现可知两思课堂能同步实现核心价值培育与化学学科核心素养培养,有效实现化学学科的育人价值。     

新手熟手初中化学教师课堂教学行为特征的比较研究*——以“酸和碱”单元教学为例

通过对新手化学教师和熟手化学教师各4节“酸和碱”单元常态课堂中教师使用教学行为链、教学行为对在时间和频次等方面的特征进行对比分析发现,在教学行为链上,新、熟手化学教师都会在较高水平的教学行为链上花费更多的时间,熟手化学教师高水平教学行为链在频次上的占比要优于新手化学教师,在不同教学行为链时间安排上的合理性要更高一些;在教学行为对上,新、熟手化学教师都多以“问”和“讲”,学生多以“答”的方式来展开课堂活动,熟手化学教师在每一次“动”和“思”上所用时间要明显高于新手化学教师,学生参与课堂的水平上,熟手化学教师要优于新手化学教师。得出如下启示:与熟手化学教师相比,新手化学教师应有效地组织和安排课堂教学行为,注重对“酸和碱”学科内容本身及其教学的驾驭。无论是熟手还是新手化学教师均应进一步给予学生课堂参与的机会。     

Determination of the enthalpy of fusion of K<Subscript>3</Subscript>TaO<Subscript>2</Subscript>F<Subscript>4</Subscript> and KTaF<Subscript>6</Subscript>

Areas of fusion and crystallization peaks of K₃TaO₂F₄ and KTaF₆ were measured using the DSC mode of a high-temperature calorimeter (SETARAM 1800 K). On the basis of these quantities, considering the temperature dependence of the calorimeter sensitivity, values of the fusion enthalpy of K₃TaO₂F₄ at the fusion temperature of 1181 K of (43 ± 4) kJ mol⁻¹ and of KTaF₆ at the fusion temperature of 760 K of (8 ± 1) kJ mol⁻¹ were determined.     

Physicochemical foundations of synthesis of new ferromagnets from chalcopyrites A<Superscript>II</Superscript>B<Superscript>IV</Superscript>C<Stack><Subscript>2</Subscript><Superscript>V</Superscript></Stack>

The results of studying phase equilibria of ternary A^IIB^IVC^V systems have been reported. Physicochemical foundations have been developed for the synthesis of new ferromagnets with Curie temperatures above room temperature structurally compatible with basic semiconducting materials. Methods of synthesis and physicochemical properties of manganese-doped A^IIB^IVC₂^V ferromagnets have been described. The results of theoretical simulation of magnetic properties have been considered and basic approaches to the explanation of the emergence of ferromagnetism in A^IIB^IVC₂^V doped with 3d metals have been surveyed. The most promising ways to produce and study dilute magnetic semiconductors as spintronics materials have been presented.     

Determination of the enthalpy of fusion of K<Subscript>3</Subscript>NbO<Subscript>2</Subscript>F<Subscript>4</Subscript>

Areas of fusion and crystallization peaks of K₃NbO₂F₄ were measured using the DCS mode of a high-temperature calorimeter (SETARAM 1800 K). On the basis of these quantities, considering the temperature dependence of the calorimeter sensitivity, the value of the fusion enthalpy of K₃NbO₂F₄ of (98 ± 6) kJ mol⁻¹ was determined at the fusion temperature of 1257 K.     

Structure of Zn<Subscript>3</Subscript>P<Subscript>2</Subscript>

The structure of Z_n3P₂ (P 4₂/nmc, a = b = 8. 0785 Å, c = 11. 3966 Å) was solved and refined to R = 3. 2% in a precision X-ray diffraction experiment (λ-MoK _a, graphite monochromator on a primary beam, 27,496 reflections) . Interatomic distances and bond angles have been determined. The fcc lattice of the structure is built from phosphorus atoms, and the zinc atoms occupy 3/4 of all tetrahedral voids; the structure is described by two equivalent models where 1/4 occupied (by zinc atoms) and 1/4 vacant voids change places. The zinc atoms that occupy the voids following the diamond principle do not change places.Original Russian Text Copyright © 2004 by I. E. Zanin, K. B. Aleinikova, M. M. Afanasiev, and M. Yu. Antipin__________Translated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 5, pp. 889–892, September–October, 2004.     

Coefficients of thermal expansion of KPb<Subscript>2</Subscript>Cl<Subscript>5</Subscript> and RbPb<Subscript>2</Subscript>Br<Subscript>5</Subscript> crystals

The temperature dependence of unit cell parameters for monoclinic KPb₂Cl₅ and tetragonal RbPb₂Br₅ crystals was studied in the range of 100–298 K. Linear and volume thermal expansion coefficients were determined.     

“蒸馏酒”还是“发酵酒”——对《科学史导论》中“spirits” 和“distillation”的再思考

科学史奠基者乔治·萨顿在《科学史导论》第二卷的第一部分对我国宋代酿酒著作《北山酒经》予以了简要描述,出现了“spirits”“distillation”等字样;而《北山酒经》被众多学者认为其描述对象是发酵酒(黄酒)。本文从东西方蒸馏技术和相关著作的文本分析对《科学史导论》中提及的蒸馏技术和蒸馏酒存在的可能性提出了质疑。     

2,4‐Di­nitro­phenyl­hydrazones of 2,4‐di­hydroxy­benz­aldehyde, 2,4‐di­hydroxy­aceto­phenone and 2,4‐di­hydroxy­benzo­phenone

In 2,4‐di­hydroxy­benz­aldehyde 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­form­amide solvate {or 4‐[(2,4‐di­nitro­phenyl)­hydrazono­methyl]­benzene‐1,3‐diol N,N‐di­methyl­form­amide solvate}, C₁₃H₁₀N₄O₆·C₃H₇NO, (X), 2,4‐di­hydroxy­aceto­phenone 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­form­am­ide solvate (or 4‐{1‐[(2,4‐di­nitro­phenyl)hydrazono]ethyl}benzene‐1,3‐diol N,N‐di­methyl­form­amide solvate), C₁₄H₁₂N₄O₆·C₃H₇NO, (XI), and 2,4‐di­hydroxy­benzo­phenone 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­acet­amide solvate (or 4‐­{[(2,4‐di­nitro­phenyl)hydrazono]phenyl­methyl}benzene‐1,3‐diol N,N‐di­methyl­acet­amide solvate), C₁₉H₁₄N₄O₆·C₄H₉NO, (XII), the molecules all lack a center of symmetry, crystallize in centrosymmetric space groups and have been observed to exhibit non‐linear optical activity. In each case, the hydrazone skeleton is fairly planar, facilitated by the presence of two intramolecular hydrogen bonds and some partial N—N double‐bond character. Each molecule is hydrogen bonded to one solvent mol­ecule.     

Effect of SO<Subscript>2</Subscript> on chlorination of Bi<Subscript>2</Subscript>O<Subscript>3</Subscript> + Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> mixtures

The reaction of Bi₂O₃ + Fe₂O₃ mixtures with chlorine and SO₂ at 250–700°C is studied. At 300–500°C, the degree of bismuth chloride sublimation from the oxide mixture increases in the presence of SO₂. Chemical sublimation of FeCl₃ occurs after BiCl₃ is virtually completely recovered from the solid phase.     

Projection of the liquidus surface of the Sb<Subscript>2</Subscript>Te<Subscript>3</Subscript>-Gd<Subscript>2</Subscript>Te<Subscript>3</Subscript>-Bi<Subscript>2</Subscript>Te<Subscript>3</Subscript> system

Phase equilibria in the Sb₂Te₃-Gd₂Te₃-Bi₂Te₃ ternary system have been studied using differential thermal analysis, namely, X-ray powder diffraction, microstructure examination, thermodynamic analysis, and microhardness and alloy density measurements. Phase diagrams of some polythermal joins and liquidus surface have been constructed. The regions of primary crystallization of phases and the coordinates of all invariant and univariant equilibria in the system under investigation have been established.