角分辨紫外光电子谱仪校正因子的测量和计算

测量并分析计算了角分辨紫外光电子谱仪的电子能量分析器的聚焦特性 ,分析计算了紫外光斜入射时光电信号的校正因子。结果表明 :偏离分析器聚焦中心 β角的光电子被分析器接收的几率为高斯函数exp( - β2 /β0 2 ) ,且 β0 =3.5° ;

光电子发射谱仪教学实验应用探索

采用光电子发射谱仪在大气环境中测试不同样品的功函数等一系列实验。光电子发射谱仪以氘灯作为紫外光源,开放式计数器作为检测器,是基于低能电子计数检测方法的仪器。实验结果表明,该仪器具有高灵敏度、方便快捷的测试特点,开辟了表面分析方法的新方法,对于新材料的设计和表征具有重要作用。在教学实验中引入功函数测试实验,培养了本科生理论与实践的结合能力,也为科研或实际生产提供了参考。

反光电子谱的自动化测量及数据处理

首次建成了国产反光电子谱仪的自动化数据采集及处理系统。整个测量装置由Apple Ⅱ微机、计数器、PIO 和A/D、D/A 卡等电路组成。

8英寸MCP型光电倍增管的实验研究

研制了一套单光电子谱测试仪。对8英寸微通道板型光电倍增管(MCP-PMT)的性能指标进行了标定,包括单光电子谱的增益和峰谷比、光电阴极的均匀性。单光电子谱测试仪采用高精度QDC采集电荷谱。VME数据获取系统积分电荷谱得到单光电子谱。采用LABVIEW的电流采样系统获得光电阴极某确定位置上光电流的I-V坪曲线。单光电子谱测试仪测得MCP-PMT在高压为2100 V、脉冲发生器的设置为脉冲宽度10 ns、采样频率1 k Hz、驱动电压1.735 V驱动LED光源时,单光电子谱的增益为2.5233×107、峰谷比值为2.78,光电阴极的非均匀性小于10%。实验测得的性能指标均满足中微子探测等实验要求。同时为20英寸MCP-PMT的成功研制奠定了理论设计及测试基础。

Ar离子辐照PET膜引起的表面结构和组分变化研究

用 35MeV u的Ar离子室温下辐照多层堆叠的半晶质的聚酯 (PET)膜 ,采用X射线衍射技术和X射线光电子谱仪分析研究了辐照引起的表面结构和组分的变化。结果表明 ,Ar离子辐照PET膜引起了明显的非晶化转变和化学键断裂 ,断键主要发生在甲氧基和羰基功能团上 ,并使这两个功能团中的C和O的比分相对减少。非晶化效应和化学键断裂同时依赖于离子的照射剂量和离子在样品表面的电子能量损失 ,剂量越高 ,表面电子能量损失越大 ,效应就明显。

Friction and Wear Performance of Magnesium Alloy against Steel under Lubrication of Rapeseed Oil with BN-containing Additive

A BN-containing additive,the boron and nitrogen modified rapeseed oil (abbreviated as BNR),was prepared by chemical modification of rapeseed oil with boric and nitrous compounds.The friction and wear performances of the AZ91D magnesium alloy against the GCr15 bearing steel under lubrication of rapeseed oil containing BNR were evaluated on a SRV tribotester.The topography and chemical species of the worn surfaces of magnesium alloy were analyzed by a scanning electron microscope (SEM) and an X-ray photoelectron spectroscope (XPS),respectively.The test results indicated that the friction and wear of the magnesium alloy-steel tribomates could be effectively reduced by incorporating BNR into the rapeseed oil lubricant.The friction coefficients and the wear scars of magnesium alloy decreased with an increasing content of BNR.The surface lubricated with the BNR-doped rapeseed oil demonstrated less wear as compared with that lubricated with neat rapeseed oil.The enhanced anti-wear and friction-reducing abilities of rapeseed oil provided by BNR in the lubrication of magnesium alloy against steel were ascribed to the formation of a composite boundary lubrication film due to the strong adsorption of BNR and rapeseed oil onto the lubricated surfaces and their tribochemical reactions with magnesium alloy.

Tribological Performances of Fatty Acyl Amino Acids Used as Green Additives in Lubricating Oil

The friction and wear characteristics of lauroyl glutamine, lauroyl glycine and lauroyl alanine, used as green additives in HVI 350 mineral lubricating oil, were evaluated on a four-ball tribotester. The morphologies and chemical species of the worn surfaces were analyzed by scanning electron microscope （SEM） and X-ray photoelectron spectroscope （XPS）, respectively. The test results indicated that the three fatty acyl amino acids could effectively improve the anti-wear and friction-reducing abilities of the HVI 350 mineral oil. The improvement in anti-wear and friction-reducing abilities of the mineral oil by the related amino acids was mainly ascribed to the formation of a composite boundary lubrication film due to the adsorption of amino acids on the friction surfaces.

Electrolyte composition and removal mechanism of Cu electrochemical mechanical polishing

The optimization of electrolytes and the material removal mechanisms for Cu electrochemical mechanical planarization(ECMP)at different pH values including 5-methyl-1H-benzotriazole(TTA),hydroxyethylidenediphosphoric acid(HEDP),and tribasic ammonium citrate(TAC)were investigated by electrochemical techniques,X-ray photoelectron spectrometer(XPS)analysis,nano-scratch tests,AFM measurements,and polishing of Cu-coated blanket wafers.The experimental results show that the planarization efficiency and the surface quality after ECMP obtained in alkali-based solutions are superior to that in acidic-based solutions,especially at pH=8.The optimal electrolyte compositions(mass fraction)are 6% HEDP,0.3% TTA and 3% TAC at pH=8.The main factor affecting the thickness of the oxide layer formed during ECMP process is the applied potential.The soft layer formation is a major mechanism for electrochemical enhanced mechanical abrasion.The surface topography evolution before and after electrochemical polishing(ECP)illustrates the mechanism of mechanical abrasion accelerating electrochemical dissolution,that is,the residual stress caused by the mechanical wear enhances the electrochemical dissolution rate.This understanding is beneficial for optimization of ECMP processes.

Friction and Wear Behaviors of Nano-Silicates in Water

Nano-metric magnesium silicate and zinc silicate with particle size of about 50-70nm were prepared in water by the method of chemical deposition. The antiwear and friction reducing abilities of the nano-silicates, as well as their composites with oleic acid tri-ethanolamine （OATEA）, were evaluated on a four-ball friction tester. The topographies and tribochemical features of the worn surfaces were analyzed by scanning electron microscope （SEM） and X-ray photoelectron spectroscope （XPS）. Results show that nano-silicates alone provide poor antiwear and friction reducing abilities in water, but exhibits excellent synergism with OATEA in reducing friction and wear. The synergism in reducing friction and wear between nano- silicates and OATEA does exist almost regardless of particte sizes and species, and may be attributed, on one hand, to the formation of an adsorption film of OATEA, and, on the other hand, to the formation oftribochemical species of silicon dioxide and iron oxides on the friction surfaces. Tribo-reactions and tribo-adsorptions of nano-silicates and OATEA would produce hereby an effective composite boundary lubrication film, which could efficiently enhance the anti-wear and friction-reducing abilities of water.

Effect of PSA tin plating process on trace lead in tin coating

In this paper,effects of conditions in phenol sulfonic acid(PSA) plating for tin coating of MR low carbon aluminum killed steel on trace Pb were examined.Trace Pb was measured by atomic absorption spectrometry(AAS)and glow discharge spectrometry,and coating morphology was observed by scanning electronic microscopy(SEM).Corrosion resistance of the tin coating was analyzed by electrochemical methods.The results indicated that Pb content in the tin coating reduced as bath temperature increased.When the temperature exceeded40 ℃,the grains in the coating were coarse and loose,reducing the corrosion resistance.As current density increased,Pb content increased rapidly,while low current density plating could lead to drain regions.The plating speed had no obvious effect on trace Pb in tin coating.In the tin plating layer,Pb was enriched at the surface and gradually reduced to zero along the depth.At bath temperature of 40 ℃ and current density of 20 A·dm^(-2),the amount of Pb could be less than 100 mg·kg^(-1) with excellent corrosion resistance.

Microstructure and microwave dielectric properties of lead borosilicate glass ceramics with Al_2O_3

The effects of Al2O3 addition on both the sintering behavior and microwave dielectric properties of PbO-B203-SiO2 glass ceramics were investigated by Fourier transform infrared spectroscope （FTIR）, differential thermal analysis （DTA）, X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The results show that with the increase of Al2O3 content the bands assigned to [SiO4] nearly disappear. Aluminum replaces silicon in the glass network, which is helpful for the formation of boron-oxygen rings. The increase of the transition temperature Tg and softening temperature Tf of PbO-B2O3-SiO2 glass ceramics leads to the increase of liquid phase precipitation temperature and promotes the structure stability in the glasses, and consequently contributes to the decreasing trend of crystallization. Densification and dielectric constants increase with the increase of Al2O3 content, but the dielectric loss is worsened. By contrast, the 3% （mass fraction） Al2O3-doped glass ceramics sintered at 725℃ have better properties of density p=2.72 g/cm3, dielectric constant Er=6.78, dielectric loss tan8=2.6×10^-3 （measured at 9.8 GHz）, which suggest that the glass ceramics can be applied in multilayer microwave devices requiring low sintering temperatures.

Process mineralogy of copper-nickel sulphide flotation by a cyclonic-static micro-bubble flotation column

In our study we investigated a refractory copper-nickel sulfide ore separation by using a cyclonic-static micro-bubble flotation column (FCSMC). The process mineralogy of the main products was studied. Using a scanning electron microscope-energy dispersive system (SEM-EDS) and an X-ray spectrometer the mineral category and content of samples were analyzed. By using a mineral liberation analyzer (MLA) the mineral liberation characteristics were revealed. It is shown that in roughing feed the monomers liberation degree of nickel pyrite and chalcopyrite take up 84.11% and 88.82%, respectively. In tailings, the lost nickel pyrite and chalcopyrite are mainly monomers. Therefore, strengthening the micro-fine particle recovery capacity is the key to increase recovery.

Corrosion Study and Passive Film Characterization of 11% Cr FIM and 15% Cr ODS Steels

An ODS （oxide dispersion strengthened） steels are one of the most notable structural materials being developed for future high-temperature energy production technologies, and several studies have been devoted to the development of ODS materials for such applications. However, only little paper focuses on corrosion behavior of F/M （ferritic martensictic） and ODS steels. The corrosion behavior of 11% Cr F/M steel and 15% Cr ODS steel were evaluated using electrochemical methods in borate buffer and 1 kmol m＂3 HNO3 with or without NaCI and also in boiling 60% nitric acid. The corrosion resistance results clearly indicated the influences of steel alloys composition and chloride ions. The XPS （X-ray photo-electron spectroscopy） results of the pre-passivated surface revealed that the oxide formed were composed predominantly of Fe203 along with Cr203, and Y203 layers in ODS steel. The corrosion rate measured in boiling nitric acid for 48 h for both the steels shows high corrosion rate in boiling condition. The SEM （scanning electron microscopy） observation of the pit morphology after corrosion tests appears with shallow pit in both steel surfaces The corrosion degradation behavior in relation to the composition of the passive oxide film in different electrolytic solutions is discussed in this paper.

Design Near-threshold Photoelectron Imaging Spectrometer Based on UV Laser Induced Photoelectron Emission Anion Source

We have developed a compact photoelectron imaging facility, including an anion source with dissociative photoelectron attachment to molecules, a linear time-of-flight mass spec-trometry （TOFMS）, and an orthogonal high-resolution threshold photoelectron velocity map imaging spectrometer （VMI）. Intense and cold cluster anions were prepared in photoelectron- attachment processes upon pulsed UV laser ablation of metal target. Combining this anion source with TOFMS-VMI, the achieved mass resolution is about 200, and the electron ki- netic energy resolution is better than 3%, i.e., 30 meV for 1 eV electrons. More importantly, low-energy photoelectron imaging spectra for CH3S- and S2- at 611.46 nm are obtained. In both cases, the refined electron affinities are determined to be 1.86264-0.0020 eV for CH3S and 1.67444-0.0035 eV for S2, respectively. Preliminary results suggest that the apparatus is a powerful tool for estimating precise electron affinities values from threshold photoelectron imaging spectroscopy.

High tap density of Ni_3(PO_4)_2 coated LiNi_(1/3)Co_(1/3)Mn_(1/3)O_2 with enhanced cycling performance at high cut-off voltage

The Li Ni1/3Co1/3Mn1/3O2 is first obtained by the controlled crystallization method and then coated with Ni3(PO4)2particles. The effects of the coating on rate capability and cycle life at high cut-off voltage are investigated by electrochemical impedance spectroscopy and galvanostatic measurements. The element ratio of Ni:Mn:Co is tested by inductively-coupled plasma spectrometer(ICP) analysis and it testified to be 1:1:1. It is indicated that Ni3(PO4)2-coated Li Ni1/3Co1/3Mn1/3O2 has an outstanding capacity retention, where 99% capacity retention is maintained after 10 cycles at 5C discharge rate between 2.7 V and 4.6 V. The electrochemical impedance spectroscopy(EIS) results show that the current exchange density i0 of the coated sample is higher than that of Li Ni1/3Co1/3Mn1/3O2, which is beneficial to its electrochemical performances. All the conclusions show that the Ni3(PO4)2coating can prominently enhance the high rate performance of the Li Ni1/3Co1/3Mn1/3O2, especially at high cut-off voltage.

A Novel γ-Alumina Supported Fe-Mo Bimetallic Catalyst for Reverse Water Gas Shift Reaction

In reverse water gas shift （RWGS） reaction COa is converted to CO which in turn can be used to pro- duce beneficial chemicals such as methanol. In the present study, Mo/AlaO3, Fe/AlaO3 and Fe-Mo/Al2O3 catalysts were synthesised using impregnation method. The structures of catalysts were studied using X-ray diffraction （XRD）, Brunauer-Emmett-Teller （BET） method, inductively coupled plasma atomic emission spectrometer （ICP-AES）, temperature programmed reduction （H2-TPR）, CO chemisorption, energy dispersive X-ray （EDX） and scanning electron microscopy （SEM） techniques. Kinetic properties of all catalysts were investigated in a batch re- actor for RWGS reaction. The results indicated that Mo existence in structure of Fe-Mo/AlzO3 catalyst enhances its activity as compared to Fe/AlaO3. This enhancement is probably due to better Fe dispersion and smaller particle size of Fe species. Stability test of Fe-Mo/AlzO3 catalyst was carried out in a fixed bed reactor and a high CO yield for 60 h of time on stream was demonstrated. Fez（MoO4）3 phase was found in the structures of fresh and used catalysts. TPR results also indicate that Fez（MoO4）3 phase has low reducibility, therefore the Fe2（MoO4）3 phase significantly inhibits the reduction of the remaining Fe oxides in the catalyst, resulted in high stability of Fe-Mo/Al2O3 catalyst. Overall, this study introduces Fe-Mo/Al2O3 as a novel catalyst with high CO yield, almost no by-products and fairly stable for RWGS reaction.

Characterization of Pyrolytic Lignin Extracted from Bio-oil

Bio-oil is a new liquid fuel produced by fast pyrolysis,which is a promising technology to convert bio-mass into liquid. Pyrolytic lignin extracted from bio-oil,a fine powder,contributes to the instability of bio-oil. The paper presents the structural features of three kinds of pyrolytic lignin extracted from bio-oil with different methods(WIF,HMM,and LMM) . The pyrolytic lignin samples are characterized by Fourier transform infrared spectrometer(FTIR) and X-ray photoelectron spectroscopy(XPS) . FTIR data indicate that the three pyrolytic lignin samples have similar functional groups,while the absorption intensity is different,and show characteristic vibra-tions of typical lignocellulosic material groups O H(3340-3380 cm-1) ,C H(2912-2929 cm-1) and C O(1652-1725 cm-1) . Comparison in the region(3340-3380 cm-1) indicates that WIF has more O H stretch groups than HMM and LMM. The carbon spectra are fitted to four peaks:C1,C C or C H,BE 283.5 eV;C2,C OR or C OH,BE 284.5-285.8 eV;C3,C O or HO C OR,BE 286.10-287.10 eV;C4,O C O,BE 287.5-287.7 eV. The absence of C1,C C or C H indicates the dominant polymerization structure of aro-matic carbon in pyrolytic lignin samples. For HMM and WIF,C2a and C2b can not be separated,so there is no free hydroxyl group in the samples. The oxygen peaks are also fitted to four peaks:O1,OH,BE = 530.3 eV;O2,RC O,BE 531.45-531.72 eV;O3,O C O,BE = 532.73-533.74 eV;O4,H2O,BE 535 eV. The absence of O1 and O4 indicates that little hydroxyl groups and adsorbed water are present in the samples.

Dissolution behavior of calcium-magnesium-silicate glass fiber

The dissolution behavior of CaO-MgO-SiO2 glass fiber was investigated by scanning electron microscopy （SEM）, Fourier-transform infrared spectrometer （FTIR） and inductively coupled plasma atomic emission spectroscopy （ICP-AES） using in-vitro tests. The results show that the soaked fiber is surrounded by an outer calcium-magnesium silicate hydrated layer, and there exists a balancing fimction between the formation and abscission of the hydrated layer during the dissolution process. The concentrations of leached ions increase constantly, and the mass loss of the fibers and pH changes of the solution are found to rise rapidly during the initial dissolution process, then their increasing rates are controlled by the balancing function of the hydrated layer at the subsequent dissolution stages. The dissolution rate constant and time for complete dissolution are estimated to be 274 ng/（cm2.h） and 15.2 d, respectively, presenting preferable biosolubilities.

Composition change and capacitance properties of ruthenium oxide thin film

Ru O2·n H2O film was deposited on tantalum foils by electrodeposition and heat treatment using Ru Cl3·3H2O as precursor.Surface morphology, composition change and cyclic voltammetry from precursor to amorphous and crystalline RuO2·n H2O films were studied by X-ray diffractometer, Fourier transformation infrared spectrometer, differential thermal analyzer, scanning electron microscope and electrochemical analyzer, respectively. The results show that the precursor was transformed gradually from amorphous to crystalline phase with temperature. When heat treated at 300 °C for 2h, RuO2·n H2O electrode surface gains mass of2.5 mg/cm2 with specific capacitance of 782 F/g. Besides, it is found that the specific capacitance of the film decreased by roughly20% with voltage scan rate increasing from 5 to 250 m V/s.

Synthesis and biochemical properties of fluorescent/magnetic bifunctional starch particles

Magnetic starch particles （MSPs） were synthesized in water-in-oil mieroemulsion at room temperature. MSPs were characterized by transmission electron microscopy （TEM）, Fourier transform infrared spectrometry （FTIR）, zeta potential system, thermogravimetric analysis （TGA） and vibrating sample magnetometry （VSM）. The average diameter of the MSPs was 220 nm, dispersed with well-proportioned size and magnetic resonance, the saturation magnetization was 3.64 A.mR/kg. MSP was coated with poly-L-lysine （PLL）, and then the surface of PLL-MSP was combined with fluorescein isothiocynate （FITC）. Results show that fluorescent/magnetic starch particles （FMSPs） are of stable photo-bleaching capability compared with free FITC, with low bio-toxicity and certain function of magnetic separation. It is expected that FMSPs are bifimctional nano-materials including fluorescence labelling and magnetic separation.