“化学实验教学论”课程中论证教学的探索——以喷泉系列实验为例

在职前教师教育类课程"化学实验教学论"中,以喷泉相关实验为例,设计论证问题和评价细则,开展论证教学的实践和探索。研究细致分析并揭示了职前教师在论证建构中存在的理由不充分,逻辑推理欠严密;忽略前提条件或特定背景;多采用直觉启发式,少采用系统分析式等问题。这为提高职前教师科学论证能力提供了参考。     

基于论证探式教学模式的高中化学教学——用化学沉淀法去除粗盐中的杂质离子

论证探究式(ADI)是科学探究活动中融入科学论证的一种教学模式。以人教版高中化学必修二教材中的实验活动“用化学沉淀法去除粗盐中的杂质离子”为例,教师从创设情境提出问题、设计方法及收集证据、构建论证、论证、反思讨论、撰写研究报告、同伴互评、报告修改与提交等8个阶段设计教学方案。ADI教学模式有利于巩固学生对化学知识的掌握,培养学生的核心素养和科学思维,提高学生的科学探究能力。     

化学教学论课程结构与教学实践研究

对于高师本科开设的化学教学论课程 ,本文给出理论课、教学技能实践课、化学教学研究、化学实验研究的课程结构 ,所依据的课程资源以及教学实践过程 ,从而形成了较完整的教学方法体系     

化学学科核心素养导向的教学实践改革思考*——基于2019版AP化学课程标准的分析

《普通高中化学课程标准(2017年版)》的颁布,开启了我国化学学科核心素养导向的教学实践的新时代。美国高中阶段实施的2019版AP化学课程凸显科学实践的课程目标,以4个化学大概念为依据选择、组织课程内容,倡导教、学、评一体化的教学策略,开展以学生为中心的引导性探究实验,设计多样化的评价任务。对比我国现行化学教学实践中缺少大规模教、学、评一体化平台,科学解释和论证能力目标外显不足,教师难以建立化学知识与学科观念素养间联系的现状,提出聚焦课程目标建设过程性评价体系,深度挖掘教学内容背后的科学解释和科学论证能力要求,深入理解知识承载的认识功能和价值等思考。     

化学生物学实验的教学实践及其安全管理

作为化学领域的新兴二级学科,化学生物学利用化学的原理、方法和具有生物活性的化合物来研究生命过程中的问题。本文主要介绍了清华大学为"学堂人才计划"学生培养建立的实验课程平台——"化学生物学实验"课程的教学实践、体会和安全管理。     

无机化学实验课程启发式教学探析

无机化学实验是高校一门重要的基础实验课程。本文介绍在无机化学实验课程中运用启发式教学法,并将其贯穿于整个教学过程。采用多种途径鼓励学生进行实践创新,引导学生深入思考,在实验中发现、探究和解决问题,提高学生的综合素质。     

高等师范院校“化学史”教学的探讨

“化学史”是高等师范院校为化学（教育）专业学生开设的一门专业选修课,但长期以来对于该门课程的教学研究不够重视。经过近几年的教学实践,在“化学史”教学过程中采用分段教学与过程评价,即参与型教学、学生试讲、学生论文及学生过程评价,取得了较好的教学效果。     

顺应时代发展,创新农药化学课程教学

顺应时代发展对农药化学教学的要求,依据现代教学论的基本原则,对农药化学课程教学进行了课堂教学-学生实验-生产实践"三位一体"的改革与实践,形成了理论学习-实验-理论学习-实践-理论学习的良性教学模式。实践表明,该模式能全面有效地提高学生创新能力和综合素质。     

《高分子化学实验》课程的教学探讨

结合本校实际情况对高分子化学实验课程的教学经验进行了探讨。在高分子化学实验的教学过程中，为充分激发学生学习的兴趣，提高学习的积极性和主动性，提高教学效果与教学质量，实验的内容首先要体现高分子化学理论课程的核心内容——高分子合成；其次实验项目要带有一定的趣味性和应用性;再次实验时间要与理论课程相协调，实验项目的安排顺序要...     

高分子化学开放性实验开设初探

为了更好的提高学生对理论课知识的学习和掌握,我们结合自身的教学实践,在高分子化学课程开设的同时开设高分子化学实验,并将开放性实验的特点“设计性、综合性”引入到高分子化学实验教学过程中。通过设计性实验使学生成为学习的主体,主动学习,达到对高分子化学理论知识深入理解和掌握;通过增加综合探究性实验,使学生对高分子化学前沿学科...     

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.     

Bis(μ‐hexa­methyl­enetetr­amine)­bis(aqua­di­bromo­cadmium)­di­aqua­di­bromo­cadmium dihydrate

The title compound, poly­[[di­aqua­di­bromo­cadmium‐μ‐(1,3,5,7‐tetra­aza­tri­cyclo[3.3.1.1^3,7]decane‐N¹:N⁵)‐aqua­cad­mium‐di‐μ‐bromo‐aqua­cadmium‐μ‐(1,3,5,7‐tetra­aza­tri­cyclo[3.3.1.1^3,7]decane‐N¹:N⁵)‐di‐μ‐bromo] dihydrate], [Cd₃­Br₆­(C₆­H₁₂­N₄)₂­(H₂O)₄]·­2H₂O, is made up of two‐dimensional neutral rectangular coordination layers. Each rectangular subunit is enclosed by a pair of Cd₃(μ₂‐Br)₆(H₂O)₃ fragments and a pair of (μ₂‐hmt)Cd(H₂O)₂Br₂(μ₂‐hmt) fragments as sides (hmt is hexa­methyl­enetetr­amine). The unique Cd^II atom in the Cd₂Br₂ ring in the Cd₃(μ₂‐Br)₆(H₂O)₃ fragment is in a slightly distorted octahedral CdNOBr₄ geometry, surrounded by one hmt ligand [2.433 (5) Å], one aqua ligand [2.273 (4) Å] and four Br atoms [2.6409 (11)–3.0270 (14) Å]. The Cd^II atom in the (μ₂‐hmt)Cd(H₂O)₂Br₂(μ₂‐hmt) fragment lies on an inversion center and is in a highly distorted octahedral CdN₂O₂Br₂ geometry, surrounded by two trans‐related N atoms of two hmt ligands [2.479 (5) Å], two trans‐related aqua ligands [2.294 (4) Å] and two trans‐related Br atoms [2.6755 (12) Å]. Adjacent two‐dimensional coordination sheets are connected into a three‐dimensional network by hydrogen bonds involving lattice water mol­ecules, and the aqua, bromo and hmt ligands belonging to different layers.     

Specific heat on Sr<Subscript>2</Subscript>Nb<Subscript>2</Subscript>O<Subscript>7</Subscript> and Sr<Subscript>2</Subscript>Ta<Subscript>2</Subscript>O<Subscript>7</Subscript>

Summary Specific heats on the single crystals of Sr₂Nb₂O₇, Sr₂Ta₂O₇ and (Sr_1-xBa_x)₂Nb₂O₇ were measured in a wide temperature range of 2-600 K. Heat anomalies of a λ-type were observed at the incommensurate phase transition of T_INC (=495 K) on Sr₂Nb₂O₇ and at the super-lattice phase transition of T_SL (=443 K) on Sr₂Ta₂O₇; the transition enthalpies and the transition entropies were estimated. Furthermore, a small heat anomaly was observed at the low temperature ferroelectric phase transition of T_LOW (=95 K) on Sr₂Nb₂O₇. The transition temperature T_LOW decreases with increasing Ba content x and it vanishes for samples of x>2%.     

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.     

Tetra­phenyl­phos­phonium 4‐hydroxy‐2,2,6,6‐tetra­methyl­piperidinyl­oxy‐4‐sulfonate

The title compound, C₂₄H₂₀P⁺·C₉H₁₇NO₅S⁻, consists of an organic monovalent cation and an organic monovalent anion, the latter being derived from the TEMPO radical (TEMPO is 2,2,6,6‐tetra­methyl­piperidin‐1‐oxyl). Two inversion‐related anions interact via two –O—H⃛O—S– hydrogen bonds, forming a dimer in which there are no short contacts between the spin centres (–N—O) of the TEMPO(OH)SO₃⁻ anions. Furthermore, no significant magnetic interaction is observed between the dimers because the dimer is surrounded by cations. These results are consistent with the paramagnetic behaviour of the title salt.     

9,10‐Di­phenyl‐9,10‐epi­dioxy­anthra­cene and 9,10‐di­hydro‐10,10‐di­methoxy‐9‐phenyl­anthracen‐9‐ol

9,10‐Di­phenyl‐9,10‐epi­dioxy­anthracene, C₂₆H₁₈O₂, (I), was accidentally used in a photo­oxy­genation reaction that produced 9,10‐di­hydro‐10,10‐di­methoxy‐9‐phenyl­anthracen‐9‐ol, C₂₂H₂₀O₃, (II). In both compounds, the phenyl rings are approximately orthogonal to the anthracene moiety. The conformation of the anthracene moiety differs as a result of substitution. Intramolecular C—H⃛O interactions in (I) form two approximately planar S(5) rings in each of the two crystallographically independent mol­ecules. The packing of (I) and (II) consists of molecular dimers stabilized by C—H⃛O interactions and of molecular chains stabilized by O—H⃛O interactions, respectively.     

Chemical durability of MoO<Subscript>3</Subscript>-P<Subscript>2</Subscript>O<Subscript>5</Subscript> and K<Subscript>2</Subscript>O-MoO<Subscript>3</Subscript>-P<Subscript>2</Subscript>O<Subscript>5</Subscript> glasses

Thermal and chemical durability studies of the phosphate glasses belonging to the binary MoO₃-P₂O₅ and the ternary K₂O-MoO₃-P₂O₅ systems are reported. The chemical resistant attack tests carried out on the free alkaline MoO₃-P₂O₅ glasses show that the glass associated with the P/Mo ratio 2 has the high chemical durability. It shows also a high glass transition temperature value. The above findings are interpreted in terms of the cross-link density of the glasses and the strength of the M-O bonds (M=P, Mo). The influence of K₂O addition on the properties (density, T _g, durability) of this binary high water resistant glass is studied. It is found that the chemical durability along with the other physical properties are reduced by the incroporation of K₂O in the glass matrix. The results were explained by assuming the formation of non-bridging oxygens and weak bonds. The mechanism of the dissolution of these glasses is proposed.     

Thermal analysis study of Bi<Subscript>2</Subscript>Sr<Subscript>2</Subscript>Ca<Subscript>2</Subscript>Cu<Subscript>3-x</Subscript>Er<Subscript>x</Subscript>O<Subscript>10+δ</Subscript> glass-ceramic system

Summary We have fabricated glasses in the Bi-2223 HT_c superconductor system with Bi₂Sr₂Ca₂Cu_3-xEr_xO_{10+ δ} nominal composition, where x=0.5 and 1.0, by the glass-ceramic technique. Using an analysis developed for non-isothermal crystallization studies, information on some aspects of crystallization temperature and thermal properties has been obtained. The crystallization studies were made using DTA with several uniform rates. The calculations of crystallization activation energies, E_a, and the Avrami parameters, n, were made based on the non-isothermal kinetic theory of Kissinger and the Ozawa’s equations. The DTA data of the samples showed that the first crystallization temperature, T_x1, increases and the second crystallization temperature, T_x2, decreases by increasing the Er concentration. This suggests that the Er substitution had significant effect on the glassification of the BSCCO material due to change on the surface nucleation and increased ionic activities at high temperature region. The activation energy for crystallization, E_a, of the samples was also showed an increase at high Er concentration case. However, the Avrami parameter, n, decreased from 2.5 to 1.7 for x=0.5 and 1.0 samples, respectively. This suggests that the growth mechanism is diffusion-controlled and three-dimensional parabolic growth takes place near the first crystallization temperature. The oxidization rates and the activation barrier for oxygen out-diffusion process, E, was calculated using the TG data. It was found that the total mass gain in the x=0.5 sample is comparably smaller than that of the x=1.0 sample. This shows that the oxygen absorption of the x=1.0 sample is faster than the x=0.5 sample, leading to increase in the oxidization rate in the x=1.0 material.     

Methyl­tri­phenyl­stibonium tetra­fluoro­borate

In the title compound, [Sb(CH₃)(C₆H₅)₃]BF₄, there are four independent cations and anions in the asymmetric unit. The geometry around the Sb atom is distorted tetrahedral, with Sb—C distances in the range 2.077 (4)–2.099 (10) Å and angles at the Sb atom in the range 103.3 (3)–119.0 (4)°.