关于中学化学中“等效平衡”教学的探讨

等效平衡是学生学习化学平衡 的一个难点,采用适当的方式,抓好这部 分教学,可以有效提高学生的学习兴趣和 思维能力.

Triangular Au-Ag framework nanostructures prepared by multi-stage replacement and their spectral properties

Triangular Au-Ag framework nanostructures （TFN） were synthesized via a multi-step galvanic replacement reaction （MGRR） of single-crystalline triangular silver nanoplates in a chlorauric acid （HAuCl4） solution at room temperature. The morphological, compositional, and crystal structural changes involved with reaction steps were analyzed by using transmission electron microscopy（TEM）, energy-dispersive X-ray spectrometry （EDX）, and X-ray diffraction. TEM combined with EDX and selected area electron diffraction confirmed the replacement of Ag with Au. The in-plane dipolar surface plasmon resonance （SPR） absorption band of the Ag nanoplates locating initially at around 700 nm gradually redshifted to 1 100 nm via a multi-stage replacement manner after 7 stages. The adding amount of HAuCl4 per stage influenced the average redshift value per stage, thus enabled a fine tuning of the in-plane dipolar band. A proposed formation mechanism of the original Ag nanoplates developing pores while growing Au nanoparticles covering this underlying structure at more reaction steps was confirmed by exploiting surface-enhanced Raman scattering （SERS）.

Theoretical Study of Reaction Paths and Transition States on Conversion Methane into C_2 Hydrocarbons Through Plasma

The direct synthesis of C2 hydrocarbons （ethylene, acetylene and ethane） from methane is one of the most important task in C1 chemistry. Higher conversion of methane and selectivity to C2 hydrocarbons can be real-ized through plasma reaction. In order to explore the reaction process and mechanism, the possible reaction paths （1）—（4） were proposed on coupling reaction of methane through plasma and studied theoretically using semi-PM3 method [PM3 is parameterization method of modified neglect of diatomic overlap （MNDO）] including determining the transition state, calculating the activation energy and thermodynamic state functions and analyzing the bond or-der and intrinsic reaction coordinate. The reaction heat results indicate that the reactions （2） and （4） are exothermic, while reactions of （1） and （3） are endothermic. The activation energy results show that activation energy for reac-tions （1） and （2） was much lower than that of reaction paths （3） and （4）. Therefore, paths （1） and （2） is the favorable reaction path energetically. More interestingly by comparing the intrinsic reaction coordinated （IRC） of the reaction paths （1） and （2）, it is found that the variations of bond lengths in reaction path （1） has a crucial effect on the poten-tial energy, while in reaction path （2）, the adjustment of the system geometry also contributes to the whole potential energy of the system.

Improved method of plasma 8-Isoprostane measurement and association analyses with habitual drinking and smoking

AIM: To develop a simple and accurate method for quantifying 8-isoprostane in plasma by employing a combination of two-step solid-phase extraction of samples and a commercially available ELISA kit, and by this method to examine the effects of drinking and smoking habits against the levels of plasma 8-isoprostane in healthy Japanese volunteers.METHODS: Plasma 8-isoprostane was extracted with ODS gel suspension followed by NH2 Sep-Pak column. The 8-isoprostane fractions were assayed using a commercially available ELISA kit. We measured plasma 8-isoprostane levels in 157 healthy Japanese volunteers divided into three groups (64 non-habitual drinkers, 56 moderate drinkers and 37 habitual drinkers) according to their alcohol consumption per week. Genotypes of aldehyde dehydrogenase 2 (ALDH2) were also determined to investigate the plasma 8-isoprostane levels with reference to drinking habits. In addition, the plasma 8-isoprostane levels of 96 non-smokers and 61 smokers from the same subjects were compared.RESULTS: Our method fulfilled all the requirements for use in routine clinical assays with respect to sensitivity, intra- and inter-assay reproducibility, accuracy and dynamic assay range. Significant increases of plasma 8-isoprostane levels were observed in female habitual drinkers when compared with those of non-habitual drinkers (t = 5.494, P < 0.0001) as well as moderate drinkers (t = 3.542, P < 0.005), and 8-isoprostane levels were also significantly different between ALDH2*2/1 and ALDH2*1/1 in the female habitual drinkers (t = 6.930, P < 0.0001), suggesting that excessive drinking of alcohol may increase oxidization stress, especially in females. On the contrary, no significant difference of the plasma 8-isoprostane levels was observed between non-smokers and smokers.CONCLUSION: Our present method was proved to be a simple and accurate tool for measuring plasma 8-isoprostane. However, the clinical utility of plasma 8-isoprostane for drinking and smoking habits was limited since elevated 8-isoprostane levels were observed in female heavy drinkers, and no association was found between smokers and nonsmokers.

Conversion of CO2 by non-Thermal Inductively-Coupled Plasma Catalysis

CO2 decomposition is a very strongly endothermic reaction where very high temperatures are required to thermally dissociate CO2.Radio frequency inductively-coupled plasma enables to selectively activate and dissociate CO2 at room temperature.Tuning the flow rate and the frequency of the radio frequency inductively-coupled plasma gives high yields of CO under mild conditions.Finally the discovery of a plasma catalytic effect has been demonstrated for CO2 dissociation that shows a significant increase of the CO yield by metallic meshes.The metallic meshes become catalysts under exposure to plasma to activate the recombination reaction of atomic O to yield O2,thereby reducing the reaction to convert CO back to CO2.Inductively-coupled hybrid plasma catalysis allows access to study and to utilize high CO2 conversion in a non-thermal plasma regime.This advance offers opportunities to investigate the possibility to use radio frequency inductively-coupled plasma to store superfluous renewable electricity into high-valuable CO in time where the price of renewable electricity is plunging.

Ammonia Removal from Wastewater through Combination of Absorption Process in the Membrane Contactor and Advance Oxydation Process in Hybride Plasma-Ozone Reactor

Wastewater containing high concentrations of ammonia can be harmful to aquatic life and degrade the water quality. Wastewater containing ammonia is usually removed by conventional methods such as aeration in towers, biological treatment and adsorption of the ammonium ion to the zeolite surface. However, these methods are less effective and relatively expensive. Therefore there is a need for alternative technologies that can improve the efficiency of ammonia removal from wastewater. This study aims to obtain the process of ammonia removal through a combination of absorption in the membrane contactor and the advance oxidation process in the hybrid plasma-ozone reactor. Wastewater containing ammonia used in the study was a synthetic wastewater with a concentration of about 800 ppm. In the experiment, the wastewater fi＇om the reservoir was firstly passed into the membrane contactor on the shell side, and then mixed with ozone from the ozonator befbre entering the plasma reactor, and finally was circulated back to the reservoir. Meanwhile, the absorbent solution was sent to the lumen fiber in membrane contactor. Experimental results showed that the ammonia removal efficiency increases with increasing in circulation rate and temperature of the wastewater. The highest efficiency of ammonia removal obtained from the experimental results was 77%.

A simple plasma reduction for synthesis of Au and Pd nanoparticles at room temperature

A simple and fast plasma reduction method is developed for synthesis of Au and Pd metal nanoparticles. The scanning electron microscopy(SEM) analysis indicates a formation of aggregates of Au and Pd nanoparticles with branched structure. The transmission electron microscopy(TEM) image shows that the inclusive nanoparticles are all about 5 nm in size. Compared to conventional hydrogen reduction method, plasma method inhibits the agglomeration of metal particles. The room temperature operation is very helpful to limit the nanoparticle size. Most interestingly, plasma reduction produces more flattened metal particles. This plasma reduction does not require the use of any hazardous reducing chemicals, showing the great potential for the fabrication of noble metal nanoparticles.

Ar/N2/CH4 Glow Discharge at Low Pressures

Ar/N2/CH4 glow discharge at low-pressure are studied in a closed system. The plasma was produced in 79.6% N2-15.4% Ar- 5.0% CH4 ternary mixture at pressures between 0.5 and 10.0 Torr. The diagnostic has been made by optical emission spectroscopy （OES）. The principal species observed were： N2, N2＋, CH＋, CN, C2, C3, HI3, Ha, C＋ and At. It presents the behaviour of the bands and lines intensities as a function of the pressure. Also, it displays the ratios of intensities of N＋2 （391.44 nm）, CN （392.08 nm）, and H （486.13 nm） to that of the N2 （337.13 rim） as function of pressure. The ratios show a slow decreasing behavior as a function of the pressure. Being the CH/N2 ratio more highest and H/N2 ratio the lowest one. The variations of excited species at different pressures may change the subsequent chemical reactions in the gas phase significantly. The present results suggest that the ion-molecule and molecule-molecule reactions in the gas phase are likely to play a dominant role in the present pressures.

Silica-gel Supported V Complexes： Preparation, Characterization and Catalytic Oxidative Desulfunzation

In this manuscript, a series of catalyst SG n-[VVO2-PAMAM-MSA] (SG silica gel, PAMAM polyamidoamine, MSA 5-methyl salicylaldehyde, n=0, 1, 2, 3) was prepared and their structures were fully characterized by Fourier transform-infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and inductive coupled plasma emission spectrometer (ICP) etc. XPS revealed that the metal V and SG n-PAMAM-MSA combined more closely after the formation of Schiff base derivatives. Their catalytic activities for oxidation of dibenzothiophene were evaluated using tert-butyl hydroperoxide as oxidant. The results showed that the catalyst SG 2.0-[VVO2-PAMAM-MSA] presented good catalytic activity and recycling time. Meanwhile, the optimal condition for the catalytic oxidation of SG 2.0-[VVO2-PAMAM-MSA] was also investigated, which showed that when the oxidation temperature was 90 °C, time was 60 min, the O/S was 3:1, and the mass content of catalyst was 1%, the rate of desulfurization could reach 85.2%. Moreover, the catalyst can be recycled several times without significant decline in catalytic activity.

The Parameters of the Stellarator as a Neutron Source for a Subcritical Reactor

The possibility of developing a stellarator-based neutron source designed for the nuclear reaction initiation in the blanket of hybrid reactor is studied. An analog of the Large Helical Device （LHD） stellarator design, with linear dimensions increased by a factor of 1.5 is taken for the magnetic system. Plasma parameters and the deuterium-tritium （DT） mixture fusion power are calculated using the space-time numerical code under the assumption of the neoclassical transport in the ambipolarity regime. Using the 10 MW plasma heating sources, it is possible to obtain the DT fusion power of one-to-two tens MW.

Surface plasmon-enhanced photochemical reactions on noble metal nanostructures

Nanoscale noble metals can exhibit excellent photochemical and photophysical properties, due to surface plasmon resonance(SPR) from specifically collective electronic excitations on these metal surfaces. The SPR effect triggers many new surface processes, including radiation and radiationless relaxations. As for the radiation process, the SPR effect causes the significant focus of light and enormous enhancement of the local surface optical electric field, as observed in surface-enhanced Raman spectroscopy(SERS) with very high detection sensitivity(to the single-molecule level). SERS is used to identify surface species and characterize molecular structures and chemical reactions. For the radiationless process, the SPR effect can generate hot carriers, such as hot electrons and hot holes, which can induce and enhance surface chemical reactions. Here, we review our recent work and related literature on surface catalytic-coupling reactions of aromatic amines and aromatic nitro compounds on nanostructured noble metal surfaces. Such reactions are a type of novel surface plasmon-enhanced chemical reaction. They could be simultaneously characterized by SERS when the SERS signals are assigned. By combining the density functional theory(DFT) calculations and SERS experimental spectra, our results indicate the possible pathways of the surface plasmonenhanced photochemical reactions on nanostructures of noble metals. To construct a stable and sustainable system in the conversion process of the light energy to the chemical energy on nanoscale metal surfaces, it is necessary to simultaneously consider the hot electrons and the hot holes as a whole chemical reaction system.

Preparation and characterization of three-dimensional micro-electrode for micro-supercapacitor based on inductively coupled plasma reactive etching technology

The capacity of supercapacitor charge storage depends on the size of the electrode surface area and the active material on the electrodes.To enhance the charge storage capacity with a reduced volume,silicon is used as the electrode material,and three-dimensional electrode structure is prepared to increase the electrode surface area on the footprint area by inductively coupled plasma reactive etching(ICP) techniques.The anodic constant current deposition method is employed to deposit manganese oxide on the electrode surface as the electroactive material.For comparison,samples without slot are prepared with a two-dimensional electrode.Scanning Electron Microscopy(SEM) and Energy Dispersive Spectroscopy(EDS) are used to characterize the surface morphology of the electrode structure and the deposited electroactive material.Electrochemical properties of the electrode are characterized by the cyclic voltammetry(CV) and the constant current charge-discharge method.Experimental results show that our approach can effectively increase the electrode surface area with more electroactive substances,and hence can increase storage capacity of the micro-supercapacitor.

Laser-driven plasma collider for nuclear studies

A novel method of initiating nuclear fusion reactions in a full plasma environment was suggested, and a proof-of-concept experiment was carried out with the D ＋D → n＋3He reaction. In this new approach, two plasma jets generated by high-intensity lasers collide headon-head. The center-of-mass energy of the nuclei increases accordingly, and therefore, reaction products can be significantly enhanced, especially in the sub-Coulomb barrier ranges. As a result of the fusion reaction, up to - 7.6 ×105 neutrons had been observed. This new type of ＂plasma collider＂ could provide an innovative tool to study nuclear reactions under astrophysical conditions.