国内外典型教材的热力学教学内容及教学思路比较

目前物理化学教学在“量子先行”和“热力学先行”两种策略的选择上依然存在争论,热力学是物理化学的重要组成部分,本文分析和比较了国内外10本典型教材在热力学教学内容安排上的现状,提出了发展方向和建议,希望对物理化学教学和教材建设提供依据。     

物理化学基础知识在化工热力学教学中的应用

化工热力学是化学工程与工艺专业的专业核心课,它与物理化学联系紧密,后者是前者学习的基础。在化工热力学新知识点的授课中,及时引导学生回顾物理化学的相关知识点并予以阐述,强调两门课程的相互渗透,将有助于学生更好地理解和掌握化工热力学知识,提高教学质量,达到更好的教学效果。本文结合物理化学和化工热力学的课堂教学实践,就物理化学中的热力学基础知识在辅助化工热力学教学过程中的应用提出了一些实例和自己的体会。     

物理化学中的热力学方法、拓展及应用

主要依托物理化学中的热力学基本原理,浅议热力学方法、简介化工热力学方法和工程热力学方法及应用等。热力学方法主要有循环法、特性函数法、变量变换法、标准状态法、平衡法及极值法、微元法等,并归纳了各种方法的特点、作用及意义。对于学生学习物理化学中的热力学,具有一定的指导意义,拓展了热力学的基本知识。     

物理化学教学内容研究交流研讨会纪要

2015年4月16~17日,高等教育出版社在山东青岛组织召开了物理化学教学内容研究交流研讨会,就自发变化和可逆过程的定义、可逆与平衡、自发与不可逆的关系、环境熵和总熵、环境的热力学界定和总熵判据、反应的方向与限度等问题进行了研讨。本文是此次会议的纪要,希望对纠正物理化学教学中的一些偏颇甚至错误的认识有所裨益。     

热力学方程在计算热力学函数中的应用

热力学方程是包含热力学基本方程、热力学状态方程以及吉布斯-亥姆霍兹方程在内的广泛的一组方程。文中对目前物理化学教材中很少提及的其他热力学状态方程进行了系统的总结和推导,同时强调理论的系统性和完整性在教学中的重要性,并在此基础上导出了物理化学教材中很少见到的吉布斯-亥姆霍兹第一方程及其在表面化学中的应用。在物理化学教学中需要特别强调特征变量的重要性,以及特征变量和化学反应条件之间的内在关系,并注意与交叉学科物理专业的热力学和统计物理学的衔接。     

关于一些热力学公式使用条件的讨论

物理化学中的热力学公式在不同条件下有不同的衍变形式,极易诱导学生产生错误理解。通过实例分析,对热力学能和焓变化计算公式、赫姆霍兹自由能和吉布斯自由能判据、热力学基本方程等的使用和理解中存在的一些问题予以讨论。     

把宏观的和微观的方法紧密结合起来建立化学热力学的新的教学体系

一、以往物理化学中化学热力学教学体系的特点以往广泛流行的物理化学中,化学热力学的教学体系一般都是以宏观的方法为主,而很少注意把宏观的方法与微观的方法结合起来。这种宏观的方法通常称之为热力学方法,以示     

完全不互溶双液系的蒸气压*

对完全不互溶双液系的饱和蒸气压进行了实验研究与理论讨论,认为完全不互溶双液系的平衡蒸气压随两组分相互溶解度减小而趋于但总是小于两纯组分的饱和蒸气压之和;当完全不互溶两液相一起静置时,上层液体能有效但不能完全阻止下层液体的挥发,这种阻止作用源于缓慢溶解、扩散和挥发这些动力学过程;提出了阻止下层液体挥发的方法,即用与之完全不互溶且密度小的液体来覆盖,并且2种液体充满容器,阴凉处密闭静置保存。     

热力学量变换的教学研究

介绍了基于热力学偏微商关系的变量变换方法,讨论了在物理化学教学中的必要性及基本要求。     

纯物质挥发能力评估的热力学分析

一个大气压下的沸点和特定温度下的饱和蒸气压常用来评估纯物质的挥发能力,但仍缺乏这2个指标为什么能够进行挥发能力评估的热力学分析。以纯液体为对象,依据热力学第二定律,建立热力学模型,对沸点和饱和蒸气压评估纯物质挥发能力的热力学本质进行了分析。同时,对在一个大气压和沸腾温度下的摩尔蒸发焓能否作为纯物质挥发能力的判据进行了热力学分析。分析表明,摩尔蒸发焓可以作为纯物质挥发能力的新评估标准。摩尔蒸发焓越小,则纯物质越容易挥发,反之亦然。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.