THE STUDY OF ADSORPTION MODEL FOR 4,4''''-BIPYRIDINE ADSORBED AT THE CHEMICALLY DEPOSITED SILVER FILM BY SERS

This paper presents the SERS spectru spectrum of 4,4'-bipyridine adsorbed at the chemically deposited silver film. Comparing with the normal Raman spectra of 4,4'-bipyridine in the solid state and in 0.5 mol/L methanol solution, we have studied the SERS spectrum and further discussed the adsorption model for 4,4'-bipyridine adsorbed at the chemically deposited silver film, and also explained the experimental results with image field mode. Experimental results show that 4,4'-bipyridine adsorbed at the chemically deposited silver film via N-atom of pyridinering (Upright).     

A SERS SPECTRA STUDY OF N-HETEROCYCLE INHIBITOR ON NON-SERS ACTIVE METAL IRON

This paper presents the SERS spectra of quinoline adsorbed on iron deposited on the silver electrode by the cathodic reaction of ferrousion. Adsorption and inhibition mechanism of quinoline were discussed by means of the SERS spectra.     

Potential Dependence of the Raman Spectra and the Study of Adsorption Model for 4, 4-Bipyridine on A Silver Electrode

The study of the adsorption properties and adsorption model of molecules or ions on substrates is an important part of surface enhanced Raman scattering (SERS) experimental investigations. In this paper, we will present the findings of our research work with regard to the potential dependence of the SERS spectra for 4, 4' -bipyridine (bpy) on the silver electrode and the adsorption model for bpy adsorbed on the silver electrode surface. We find the intensities of the SERS spectra with all Raman shifts can be changed by changing the applied potentiat and reach maxima when the applied potential is ca. -0.70 V (Vs. SCE). The experimental study also indicates that the pyridine ring of bpy adsorbs directly on the silver electrode surface via the N-atom.     

INVESTIGATION OF ADSORPTION AND ORIENTATION OF PYRIDINE DERIVATIVES ON IRON BY SERS SPECTROSCOPY

Surface enhanced Raman scattering (SERS) spectra of pyridine derivatives adsorbed on iron in 0.1mol/L solution at pH=3.4 were measured using an activated silver electrode covered with an appropriate amount of electrode posited iron. Since bands at 220cm-1,250cm-1 and 240cm-1 in the SERS spectra of pyridine derivatives on iron were, assigned to Fe-N bond, it was concluded, that the derivatives molecules were chemisorbed on the iron surface by the formation of iron-nitrogen coordinated bond inhibiting the corrosion of iron metal.     

Research of Inclusion Complexation of 4,4'-Thiodiphenol Effected by β-Cyclodextrin in Aqueous Solutions and the Effect on Photodegradation

The inclusion behavior of 4,4′ -Thiodiphenol (TDP),a typical bisphenol and endocrine disruptor,reacts with β-cyclodextrin (β-CD) in aqueous solutions has been investigated by means of UV absorption spectrum and quantum-chemical calculation with Gaussian 98 software. The results show that the inclusion behavior of TDP is quite different in acidic solutions (pH 5.9) from that in alkaline solutions (pH 10.0). This behavior difference is attributed to the different formula structures in aqueous solutions at acidic and alkaline pH values that are demonstrated by quantumchemical modeling and calculation. TDP forms a 1∶1 β-CD inclusion complex in aqueous solutions. The equilibrium constant K was calculated to be 553.49 L/mol at pH 5.9 and 1 318.20 L/mol at pH 10.0 respectively for the inclusion complex reaction by using the modified Benesi-Heldbrand equation. After inclusion TDP's structure is changed especially at the inclusion part with the bond order becoming larger,which results in inhibitive photodegradation during direct photooxidation and H2O2 assisted photooxidation.     

Topography,structure, and formation kinetic mechanism of carbon deposited onto nickel in the temperature range from 400 to 850℃

The carbon deposition behavior on nickel particles was observed within the temperature range from 400 to 800℃ in a pure methane atmosphere. The topography, properties, and molecular structure of the deposited carbon were investigated using field-emission scanning electron microscopy (FESEM), temperature-programmed oxidation (TPO) technology, X-ray diffraction (XRD), and Raman spectroscopy. The deposited carbon is present in the form of a film at 400-450℃, as fibers at 500-600℃, and as particles at 650-800℃. In addition, the structure of the deposited carbon becomes more ordered at higher temperatures because both the TPO peak temperature of deposited carbon and the Raman shift of the G band increase with the increase in experimental temperature, whereas the intensity ratio between the D bands and the G band decreases. An interesting observation is that the carbon deposition rate is suppressed in the medium-temperature range (M-T range) and the corresponding kinetic mechanism changes. Correspondingly, the FWHM of the G and D1 bands in the Raman spectrum reaches a maximum and the intensities of the D2, D3, and D4 bands decrease to low limits in the M-T range. These results indicate that carbon structure parameters exhibit two different tendencies with respect to varying temperature. Both of the two group parameters change dramatically as a peak function with increasing reaction temperature within the M-T range.     

Topography,structure,and formation kinetic mechanism of carbon deposited onto nickel in the temperature range from 400 to 850°C

The carbon deposition behavior on nickel particles was observed within the temperature range from 400 to 800°C in a pure methane atmosphere.The topography,properties,and molecular structure of the deposited carbon were investigated using field-emission scanning electron microscopy(FESEM),temperature-programmed oxidation(TPO) technology,X-ray diffraction(XRD),and Raman spectroscopy.The deposited carbon is present in the form of a film at 400–450°C,as fibers at 500–600°C,and as particles at 650–800°C.In addition,the structure of the deposited carbon becomes more ordered at higher temperatures because both the TPO peak temperature of deposited carbon and the Raman shift of the G band increase with the increase in experimental temperature,whereas the intensity ratio between the D bands and the G band decreases.An interesting observation is that the carbon deposition rate is suppressed in the medium-temperature range(M-T range) and the corresponding kinetic mechanism changes.Correspondingly,the FWHM of the G and D1 bands in the Raman spectrum reaches a maximum and the intensities of the D2,D3,and D4 bands decrease to low limits in the M-T range.These results indicate that carbon structure parameters exhibit two different tendencies with respect to varying temperature.Both of the two group parameters change dramatically as a peak function with increasing reaction temperature within the M-T range.     

Temperature dependence of surface enhanced Raman scattering on C<Subscript>70</Subscript>

The temperature dependence of surface enhanced Raman scattering of the C70 molecule is reported. The Raman scattering of C70 molecules adsorbed on the surface of a silver mirror was measured at different temperatures. The experimental results indicate that the relative intensities of the Raman features vary with the temperature of the sample. When the temperature decreases from room temperature to 0℃, the relative intensifies of certain Raman bands decrease abruptly. If we like the strongest band 1565cm^-1 as a standard value 100, the greatest decrease approaches to 43%. However, with the further decrease in the temperature these relative intensities increase and resume the value at room temperature. And such a temperature dependence is reversible. Our results show that the adsorption state of the C70 molecules on the silver surface around 0℃ changes greatly with the temperature, resulting in a decrease in relative intensities for some main Raman features of C70 molecule. When the temperature is lower than 0℃, the adsorption state changes continually and more slowly. Synchronously, eight new Raman features, which have not ever been reported in fiterature, are observed in our experiment and this enriches the basic information of the vibrational modes for C70 molecule.     

AN APPROACH TO CALCULATE THE SURFACE TENSION OF THE LIQUID NITROGEN FILM ON SOLIDS FROM AN ADSORPTION ISOTHERM

The equations, used in this paper to calculate the surface tension of the liquid nitrogen film formed by the physical adsorption on many different model solids (e.g. spherical partiele, plane particle and spherical cavity pores or cylindrical pores at the openings of both ends in solid bodies), have been derived on the thermodynamie principle. The calculated results have shown that the surface tension (γ) of the adsorbed liquid nitrogen film on most of non-porous solid surfaces diminishes with the rise of the nitrogen gas pressure (p) or of the adsorbed layers (n) at 77.3K; when p reaches the vapour pressure (p_s) of the bulk liquid nitrogen, y turns into the surface tension (γ_o) of the bulk liquid nitrogen; whgn p /p, <0.98, there is an obvious difference between γ and γ_O.     

Effects of specific surface area of metallic nickel particles on carbon deposition kinetics

Carbon deposition on nickel powders in methane involves three stages in different reaction temperature ranges. Temperature programing oxidation test and Raman spectrum results indicated the formation of complex and ordered carbon structures at high deposition temperatures. The values of I(D)/I(G) of the deposited carbon reached 1.86, 1.30, and 1.22 in the first, second, and third stages, respectively. The structure of carbon in the second stage was similar to that in the third stage. Carbon deposited in the first stage rarely contained homogeneous pyrolytic deposit layers. A kinetic model was developed to analyze the carbon deposition behavior in the first stage. The rate-determining step of the first stage is supposed to be interfacial reaction. Based on the investigation of carbon deposition kinetics on nickel powders from different resources, carbon deposition rate is suggested to have a linear relation with the square of specific surface area of nickel particles.     

Study on wind characteristics of typhoon muifa on the sutong bridge

As a cable-stayed bridge with the longest main span, the Sutong Bridge faces the threat of typhoons every year. Based on field measured data measured at the top of the tower and at the mid-span by anemometers, Typhoon Muifa is analyzed in detail to obtain the wind characteristics, including the mean wind speed and direction, turbulence intensity and gust factor, power spectral density and integral scale of turbulence, etc. The correlated mean wind speeds at the two heights show the reliability of recorded wind data as well as the variation of wind speed with height. Turbulence intensities and gust factors fluctuate in a similar way. The values of integral scales are sensitive in different case. The measured power spectra are particularly compared with Kaimal spectrum, Teunissen spectrum, Harris spectrum, and Davenport spectrum. The results show that the measured spectra cannot fit the code-suggested spectra very well, which exhibits the demand of more accurate spectra. Conclusions obtained in this article can provide references for wind resistance design of super-long-span cable-stayed bridges.     

Carbon deposition in porous nickel/yttria-stabilized zirconia anode under methane atmosphere

A commercial solid oxide fuel cell with a Ni/YSZ anode was characterized under a pure methane atmosphere. The amount of deposited carbon increased with an increase in temperature but decreased when the temperature exceeded 700°C. The reactivity of carbon decreased with increasing deposition temperature. Filamentous carbon was deposited from 400 to 600°C, whereas flake carbon was deposited at 700 and 800°C. With increasing temperature, the intensity ratio of the D band over the sum of the G and D bands was constant at the beginning and then decreased with the transformation of the carbon morphology. The crystallite size increased from 2.9 to 13 nm with increasing temperature. The results also indicated that the structure of the deposited carbon was better ordered with increasing deposition temperature. In comparison with pure Ni powders, the interaction between the YSZ substrate and Ni particles could not only modify the carbon deposition kinetics but also reduce the temperature effect on the structure and reactivity variation of carbon.     

Characterization of low-purity clays for geopolymer binder formulation

The production of geopolymer binders from low-purity clays was investigated. Three low-purity clays were calcined at 750℃ for 4 h. The calcined clays were chemically activated by the alkaline solutions of NaOH and Na₂SiO₃. The compressive strength was measured as a function of curing time at room temperature and 85℃. The results were compared with those of a pure kaolin sample. An amorphous aluminosilicate polymer was formed in all binders at both processing temperatures. The results show that, the mechanical properties depend on the type and amount of active aluminum silicates in the starting clay material, the impurities, and the processing temperature.     

Mechanical,electrical, and thermal expansion properties of carbon nanotube-based silver and silver-palladium alloy composites

The mechanical, electrical, and thermal expansion properties of carbon nanotube (CNT)-based silver and silver-palladium (10:1, w/w) alloy nanocomposites are reported. To tailor the properties of silver, CNTs were incorporated into a silver matrix by a modified molecular level-mixing process. CNTs interact weakly with silver because of their non-reactive nature and lack of mutual solubility. Therefore, palladium was utilized as an alloying element to improve interfacial adhesion. Comparative microstructural characterizations and property evaluations of the nanocomposites were performed. The structural characterizations revealed that decorated type-CNTs were dispersed, embedded, and anchored into the silver matrix. The experimental results indicated that the modification of the silver and silver-palladium nanocomposite with CNT resulted in increases in the hardness and Young’s modulus along with concomitant decreases in the electrical conductivity and the coefficient of thermal expansion (CTE). The hardness and Young’s modulus of the nanocomposites were increased by 30%–40% whereas the CTE was decreased to 50%–60% of the CTE of silver. The significantly improved CTE and the mechanical properties of the CNT-reinforced silver and silver-palladium nanocomposites are correlated with the intriguing properties of CNTs and with good interfacial adhesion between the CNTs and silver as a result of the fabrication process and the contact action of palladium as an alloying element.     

Spatial separation of spectrum inside the tapered metamaterial optical waveguide

In this work,the optical metamaterials based on silver dendritic cells are prepared by electrochemical deposition,and its transmission and focusing behaviors are investigated.The experimental results show that the optical metamaterials reveal a multiple pass-band transmission spectrum and a prominent focusing effect at the wavelength corresponding to the maximum transmission coefficient.Two optical metamaterial samples are combined into a tapered optical waveguide,and the spectra of transmitted light at the surface of the tapered optical waveguide is measured by using the fiber spectrometer along the light propagation direction.The results demonstrate that each frequency component of the wave packet is stopped at a different waveguide thickness,leading to the spatial separation of its spectrum.The spatial separation of spectrum can be effectively tuned by adjusting the inclination of the tapered optical waveguide,which can be used for storing photons and slow-light research.     

Phase-field simulation on microstructure evolution of D0_(19) phase in γ/γ′structure of Co–Al–W superalloys

The morphological evolution and precipitation kinetics of γ′ and D0_(19)(Co_3 W) phase in Co–Al–W alloys at 900 °C have been studied by applying Phase-field method and experiment in order to understand the transformation process of γ′ phase and D0_(19) phase. The growth processes of D0_(19) phase and precipitation of γ′ phase under elastic fields were simulated through coupling with thermodynamics and dynamics databases. The simulation results indicate that the misfit δ≥ 0.53% has a greater impact on γ′ particle morphology in γ/γ′ structure.Co–Al–W alloy with low Al and high W is one of the factors to promote the precipitation of D0_(19) phase. Three stages during aging, namely the γ′ phase incubation stage, the γ′ phase fast nucleation and growth stage, and the transformation from γ′ phase to D0_(19) phase stage can be observed with the non-constant coarsening rate that varying with the decrease of γ′ phase. The particle size distribution(PSD) during the precipitation of D0_(19) phase is more in line with MLSW theory than LSW theory. This simulation results are in good agreement with the experiment results to help analyze microstructure evolution of Co–Al–W alloy.     

Effect of Ti and Al on microstructure and partitioning behavior of alloying elements in Ni-based powder metallurgy superalloys

The microstructure and partitioning behaviors of alloying elements in the γ and γ′ phases in Ni-based powder metallurgy superalloys with different Ti and Al contents were investigated. The results showed that Ti and Al were mainly enriched in the γ′ phase, partially partitioned in the γ matrix, and slightly distributed in the carbides. Different Ti and Al contents in various alloys influenced the composition and amount of MC carbides but did not influence the MC carbides' morphology. With increasing Ti and Al contents, γ + γ′ fan-type structures formed at the grain boundary, eventually resulting in a coarsened γ′ phase. In addition, the morphology of the secondary γ′ phase transformed from nearly spherical to cuboidal. The saturation degrees of Cr, Co, and Mo in the γ matrix were substantially improved with increasing Ti and Al contents.     

Different mechanisms between reactions of soot with gaseous and adsorbed NO2

The reactions of soot with gaseous and adsor- bed NO2 were tested over the K/MgA1O catalyst. After the reaction intermediates were identified by combination of in situ IR characterization and first-principles calculation, the different mechanisms were elucidated. It was found that the reactivity of adsorbed NOa is lower than that of the gas form. The adsorbed NOe reacts with soot in the form of nitrates, leading to the observation of two IR bands at 2,234 and 2,110 cm-1, which are ascribed to the vibration fre- quencies of cyanates on K sites and cyanides on the MgAlO support, respectively. On the contrary, the isocy- anates were confirmed as intermediates in the reaction of soot with gaseous NO2. Because the adsorbed NOe species （i.e., nitrates） are restricted by the electrostatic field of K＋, the cyanates are produced and readily cracked into cya- nides, which transfer to the MgAlO support. The gaseous NO2 favours the production of isocyanates due to their higher stability. The weaker reactivity of adsorbed NO2 at lower temperatures can be attributed to the restriction of the electrostatic field of K＋.     

银在M-掺杂石墨烯上吸附的第一性原理计算

Graphene is an ideal reinforcing phase for a high-performance composite filler, which is of great theoretical and practical significance for improving the wettability and reliability of the filler. However, the poor adsorption characteristics between graphene and the silver base filler significantly affect the application of graphene filler in the brazing field. It is a great challenge to improve the adsorption characteristics between a graphene and silver base filler. To solve this issue, the adsorption characteristic between graphene and silver was studied with first principle calculation. The effects of Ga, Mo, and W on the adsorption properties of graphene were explored. There are three possible adsorbed sites, the hollow site (H), the bridge site (B), and the top site (T). Based on this research, the top site is the most preferentially adsorbed site for Ag atoms, and there is a strong interaction between graphene and Ag atoms. Metal element doping enhances local hybridization between C or metal atoms and Ag. Furthermore, compared with other doped structures (Ga and Mo), W atom doping is the most stable adsorption structure and can also improve effective adsorption characteristic performance between graphene and Ag.     

THE STUDY OF ADSORPTION MODEL OF SOME CHEMICALS ADSORBED ON A SILVER ELECTRODE

This paper presents the study of the competi tire and cooperarive adsorption characteristics of pyridine and benzoic acid molecules (ions) on the electrochemically roughened surface of the silver electrode by SERS.