物理情境虽异 解题方法类同——介绍两相互作用物体类问题的解法

要学好物理,有效提高解题能力.其中一条就是要掌握典型物理问题的求解方法.这样有利于学生举一反三,有效地提高解题的能力.在整个高中阶段物理教学中,这样的例子很多.现就两相互作用物体类问题的解法举例如下.

尽量让学生在玩中学 学中玩——谈谈“物体的相互作用”的探究性教学

以“物体的相互作用”为例，讨论了如何进行探究性教学．

A New Model on Origin and Evolution of Biology

Modified classical Boltzmann entropy as generalized entropy, then proposed Maximum Generalized Entropy Principle fusing physics and biology, and established a new model for biological origin and evolutions based on this principle, finally took protein evolution for an example to analyze. The model provided some reference for biological complexity research.

系统的动能定理

在高中阶段,动能定理一般只应用于单个物体,但动能定理也可应用于两个或两个以上的物体组成的系统,而且有时会使要解决的问题变得更为简单。但应用于系统时,应注意总功包括系统中所有物体相互作用的内力和系统外力做功的代数和,此时动能定理可表述为:系统中所有物体相互作用的内力和系统外力做的总功等于系统动能的增加,即:W外+W内=△Ek。

Effect of Cr(Ⅵ) and p-Chloroaniline Interaction on Their Reaction Behaviors on Soil Colloids

Adsorption of Cr(Ⅵ) and p-chloroaniline on three typical soil colloids and pH influence were studied using batch equilibrium method. Both of Cr(Ⅵ) and p-chloroaniline adsorption on the colloids could be well described by general adsorption simulation equations. The adsorption processes changed with media pH. When Cr(Ⅵ) and p-chloroaniline coexisted on soil colloids, their interactions could be observed in a certain pH range to be accompanied with Cr(Ⅵ) reduction, which clearly suggested that a surface catalytic reaction occurred in this system. Soil colloid acted as an efficient catalyst for the interaction of Cr(Ⅵ) and p-chloroaniline. The pH values at which no interaction was observed were 4.0, 4.5 and 5.0 for the colloids of indigotic black soil, yellow-brown soil and latosol, respectively. Capillary electrophoresis used to analyze p-chloroaniline provided a high separation efficiency and short separation time, and needed no more extensive pretreatment of samples.

Boosting chiral carboxylic acid hydrogenation by tuning metal-MO_(x)-support interaction in Pt-ReO_(x)/TiO_(2) catalysts

Engineering the surface microenvironment by tuning the binary interactions between a supported metal with a secondary metal oxide(MO_(x))or support has been a common method for improving the catalytic performance of supported metal catalysts.However,few studies have investigated the ternary interactions among the metal,MO_(x),and support.Here,we report for the first time the formation of metal-MO_(x)-support interaction(MMSI)in reducible TiO_(2)-supported PtReO_(x) catalysts,affording 87% yield and 100% ee in the tandem hydrogenation of an aqueous chiral cyclohexane-1,2-dicarboxylic acid into the corresponding diol;the catalytic activity is eight times higher than that obtained with non-reducible support counterparts in the same reaction via traditional batch synthesis with multiple steps and unfriendly reagents.Detailed experimental and computational studies suggest that the TiO_(2) crystalline phase-dependent density of the oxygen vacancies induces different Pt-ReO_(x)-TiO_(2) interactions,which dominate the electron transfer therein and tune the adsorption strength of the carbonyl moiety of the substrate/intermediate,thus promoting the hydrogenation activity and selectivity.In addition,the strong MMSI endows the optimal rutile TiO_(2) supported PtReO_(x) catalyst with an outstanding lifetime of 400 h in a fixed-bed reactor under acidic aqueous conditions and ensures efficient applications in the selective hydrogenation of aliphatic dicarboxylic acids and functional carboxylic acids.This work provides a promising strategy for the development of efficient and stable supported catalysts for the selective hydrogenation of diverse C-O and C=O bonds.

A New Energy Concept

According to the uncertainties in the results and the wide diversity of how to approach the subject, a new concept for energy is proposed： Energy is an exchange between two different concentrations, the concentration of time in space outside what we call matter and the concentrated phase of time in matter space which is the matter itself. The concept of motion for energy is replaced by time-space interactions with time taken as solid matter. Motion enhances the exchange between the mass and its surrounding time in space, annihilation and creation are special forms of this exchange. During the motion of a mass, it increases as a result of this dissolution. Time concentration in Fock space is responsible for the collision phenomena in physics. In this paper, a new mathematical operator （the equal operator） is introduced.

Transport Properties of Ferrite Perovskite Material

Transport properties of LaFeO3 in the temperature range of 2 K 〈 T 〈 300 K have been explored for the first time using interaction potential developed by the author and found that our computed results on transport properties follow the same trend as that of available experimental values. These are scientifically and technologically important materials with orthorhombic perovskite-like structure and space group Pbnm. Lanthanum ferrite, LaFeO3 is semiconducting and antiferrom agnetically ordered at zero. The thermodynamics of perovskite-type or related materials of potential use in, e.g., solid oxide fuel cells have been studied to a rather limited extent only.

Manifestation If Substance Molecular Structure in Temperature Effects of Light Scattering

DCMSL （depolarization components of molecular scattering of light） have been studied within the wide spectral range （0-200 cm-1） and in the temperature intervals （20-200 ℃） in toluol （C6HsCH3） and aniline （C6HsNH2）. It has been shown that when a liquid is heated and temperatures approach to critical ones, a significant contribution of DCMSL is made by vibration motion of molecules. The special properties of the temperature-frequency behavior of DCMSL spectra are discussed from the view point of hindered rotation of liquid molecules with consideration of intermolecular interaction.

The green fuel from carbon waste： optimization and product selectivity model studies

Increase in greenhouse gases, has made scientists to substitute alternative fuels for fossil fuels. Nowadays, converting biomass into liquid by Fischer-Tropsch synthesis is a major concern for alternative fuels （gasoline, diesel etc.）. Selectivity of Fischer-Tropsch hydrocarbon product （green fuel） is an important issue. In this study, the experimental data has been obtained from three factors; temperature, H2/CO ratio and pressure in the fixed bed micro reactor. T = 543-618 （K）, P = 3-10 （bar）, H2/CO = 1-2 and space velocity = 4500 （l/h） were the reactor conditions. The results of product modeling for methane （CH4）, ethane （C2H6）, ethylene （C2H4） and CO conversion with experimental data were compared. The effective parameters and the interaction between them were investigated in the model. H2/CO ratio and pressure and interaction between pressure and H2/CO in ethane selectivity model and CO conversion and interaction between temperature and H2/CO ratio in methane selectivity model and ethylene gave the best results. To determine the optimal conditions for light hydrocarbons, ANOVA and RSM were employed. Finally, products optimization was done and results were concluded.

The Conquest of the Mars

The exploration of Mars, alike of other planets, would be oriented on a so called on-line tracking. At this approach the development of structural indicators can be followed at time using geological receptors. The principle on what stays this exploration stems from the fact, that a planet is an object, where interactions among its elements are to some extent organized. It means that it goes about an object with a hidden system of control aiming to augment its level of existence and that it is not a ＂stack of stones＂. In advance it is necessary to establish some ways-out for the on-line tracking. The first way-out is the fact, that this is an object been monitored, it means a system of organized elements, which has its proper existence and its strategies for a cultivation of this existence. These elements are primarily atoms and for a monitoring of their activities it is possible to use their complexes, e.g. crystals and of course occasionally higher structures, too. Another way-out is the fact, that elements have their proper satisfaction and successfulness and that on basis of those quantities stays the existence of the overall object. These quantities are for new observable mainly on higher structures.

Chemical Physics in Living Cells-using Light to Visualize and Control Intracellular Signal Transduction

Cells are crowded microenvironments filled with macromolecules undergoing constant phys- ical and chemical interactions. The physicochemical makeup of the cells aff）cts various cellular responses, determines cell-cell interactions and influences cell decisions. Chemical and physical properties diff）r between cells and within cells. Moreover, these properties are subject to dynamic changes in response to environmental signals, which often demand adjustments in the chemical or physical states of intracellular molecules. Indeed, cellular responses such as gene expression rely on the faithful relay of information from the outside to the inside of the cell, a process terrned signal transduction. The signal often traverses a complex path across subcellular spaces with variable physical chemistry, sometimes even influencing it. Understanding the molecular states of such signaling molecules and their intracellular environments is vital to our understanding of the cell. Exploring such intricate spaces is possible today largely because of experimental and theoretical tools. Here, we focus on one tool that is commonly used in chemical physics studies light. We summarize recent work which uses light to both visualize the cellular environment and also control intracel- lular processes along the axis of signal transduction. We highlight recent accomplishments in optical microscopy and optogenetics, an emerging experimental strategy which utilizes light to control the molecular processes in live cells. We believe that optogenetics lends un- precedented spatiotemporal precision to the manipulation of physicochemical properties in biological contexts. We hope to use this work to demonstrate new opportunities for chemical physicists who are interested in pursuing biological and biomedical questions.

Recent advances in molecular basis for strigolactone action

Strigolactones （SLs） are a very special class of plant hormones, which act as endogenous signals to regulate shoot branching in plants, and also serve as rhizosphere signals to regulate interactions of host plants with heterologous organisms such as symbiotic arbuscular mycorrhizal fungi and parasitic weeds. In this short review, we give a brief description of novel discoveries in SL biosynthesis pathway, and mainly summarize the recent advances in SL perceotion and signal transduction.

Synthesis of amphiphilic poly(fluorene) derivatives for selective imaging of Staphylococcus aureus

Three amphiphilic poly（fluorene-co-phenylene） derivatives with different side chains （PFP-I, PFP-2, PFP- 3） were designed and synthesized for exploring their detection and imaging of pathogens. Upon incuba- tion with six kinds of different pathogens, it was found the three polymers could selectively interact with Staphylococcus oureus （S. aureus）. Their selective imaging towards S. aureus were thus realized. The selective imaging towards S. aureus was also confirmed even under the blend of microbes. PFP-3 shows stronger fluorescence imaging signal than PFP-1 and PFP-2. Zeta potential and isothermal titration microcalorimetry （ITC） tests demonstrated that both electrostatic interactions and hydrophobic interac- tions played important roles in the binding between PFPs and pathogens. Thus, amphiphilic PFP-3 exhi- bits great potential for specific imaging ors. aureus in a simple and rapid manner.