利用计算机自动计算固液气相面的接触角

本文利用边缘提取和曲线拟合的算法求取组元界面的动态变化参数，从而实现对所摄图象自动计算固液气相面的接触角和分析固液气相面的润湿特性。

铁水凝固界面前沿中夹杂物与气泡行为研究

在固—液界面前沿的富集层中，由于界面的张力差，引起粒子的运动，粒子的运动速度计算公式为：Ｖ＿ｌ＝（４／９ηＤ＿Ｌ）（１－Ｋ＿Ｅ）Ｃ＿ｏ（ｄ＿σ／ｄＣ＿Ｌ）ＲＶｓ×［１－（９／８）Ｒ（ｘ－Ｒ）］￣（－１）ｅｘｐ［－Ｖ＿ｓ（ｘ－δ）／Ｄ＿Ｌ］，用此公式分析了Ｆｅ－Ｏ、Ｆｅ－Ｔｉ、Ｆｅ－Ｓ等富集层中，Ａｌ＿２Ｏ＿３夹杂物与气泡的状态，阐明了粒子运动速度、铁水量、溶质度、夹杂物及气泡半径等的关系。分析表明，由于氧、钛、硫溶质的浓度差，小的Ａｌ＿２Ｏ＿３夹杂物或气泡向固相面运动并与之接触，夹杂物与气泡的运动速度随氧、钛、硫溶质浓度的增大而提高。

Low temperature solid-phase sintering of sintered metal fibrous media with high specific surface area

A procedure of low temperature solid-phase sintering（LTSS） was carried out to fabricate sintered metal fibrous media（SMFM） with high specific surface area.Stainless steel fibers which were produced by cutting process were first plated with a coarse copper coating layer by electroless plating process.A low-temperature sintering process was then completed at about 800 °C for 1 h under the protection of hydrogen atmosphere.The results show that a novel SMFM with complex surface morphology and high specific surface area（0.2 m2/g） can be obtained in this way.The effect of sintering temperature on the surface morphology and specific surface area of SMFM was studied by means of scanning electron microscopy and Brunauer-Emmett-Teller.The damage of micro-structure during the sintering process mainly contributed to the loss of specific surface area of SMFM and the optimal sintering temperature was 800 °C.

Study of NiSi/Si Interface by Cross-Section Transmission Electron Microscopy

Different silicidation processes are employed to form NiSi,and the NiSi/Si interface corresponding to each process is studied by cross-section transmission electron microscopy （XTEM）. With the sputter deposition of a nickel thin film,nickel silicidation is realized on undoped and doped （As and B） Si（001） substrates by rapid ther mal processing （RTP）. The formation of NiSi is demonstrated by X-ray diffraction and Raman scattering spectros- copy. The influence of the substrate doping and annealing process （one-step RTP and two-step RTP） on the NiSi! Si interface is investigated. The results show that for one-step RTP the silicidation on As-doped and undoped Si substrates causes a rougher NiSi/Si interface,while the two-step RTP results in a much smoother NiSi/Si interface. High resolution XTEM study shows that axiotaxy along the Si（111） direction forms in all samples, in which specific NiSi planes align with Si（111） planes in the substrate. Axiotaxy with spacing mismatch is also discussed.

"Environmental phosphorylation"boosting photocatalytic CO_(2)reduction over polymeric carbon nitride grown on carbon paper at air-liquid-solid joint interfaces

The limited CO_(2)content in aqueous solution and low adsorption amount of CO_(2)on catalyst surface lead to poor photocatalytic CO_(2)reduction activity and selectivity.Herein,the design and fabrication of a novel photocatalytic architecture is reported,accomplished via chemical vapor deposition of polymeric carbon nitride on carbon paper.The as-obtained samples with a hydrophobic surface exhibit excellent CO_(2)transport and adsorption ability,as well as the building of triphase air-liquid-solid(CO_(2)-H_(2)O-catalyst)joint interfaces,eventually resulting in the inhibition of H2 evolution and great promotion of CO_(2)reduction with a selectivity of 78.6%.The addition of phosphate to reaction environment makes further improvement of CO_(2)photoreduction into carbon fuels with a selectivity of 93.8%and an apparent quantum yield of 0.4%.This work provides new insight for constructing efficient photocatalytic architecture of CO_(2)photoreduction in aqueous solution and demonstrates that phosphate could play a key role in this process.

Effect of Gd_(0.2)Ce_(0.8)O_(1.9) nanoparticles on the oxygen evolution reaction of La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ) anode in solid oxide electrolysis cell

La（0.6）Sr（0.4）Co（0.2）Fe（0.8）O（3-δ）（LSCF） anodes were infiltrated by Gd（0.2）Ce（0.8）O（1.9）GDC） nanoparticles to improve the oxygen evolution reaction（OER） performance of solid oxide electrolysis cells（SOECs） in CO2 electroreduction. The effect of GDC loading was investigated, and 10 wt% GDC nanoparticle infiltration of the LSCF（10 GDC/LSCF） anode results in the highest OER performance. Electrochemical impedance spectra measurements indicate that the infiltration by GDC nanoparticles greatly decreases the polarization resistance of the SOECs with the 10 GDC/LSCF anodes. The following distribution of relaxation time analysis suggests that four individual electrode processes are involved in the OER and that all of them are accelerated on the 10 GDC/LSCF anode. Three phase boundaries, surface oxygen vacancies, and bulk oxygen mobility increased, based on scanning electron microscopy and temperature-programmed desorption of O2 characterizations, and contributed to the enhancement of the four electrode processes of the OER and electrochemical performance of SOECs.

Vertical section phase diagrams of La−Fe−B ternary system

The vertical sections of the La−Fe−B system were investigated using electron probe microanalysis and differential thermal analysis.Based on the microstructures and phase compositions of the as-cast and equilibrium alloys,together with their heat flow−temperature curves,phase diagrams for three vertical sections were drawn:La_(x)Fe_(82)B_(y)(x+y=18),La_(x)Fe_(70)B_(y)(x+y=30)and La_(x)Fe_(53)B_(y)(x+y=47),where x and y represent mass fraction of La and B,respectively,%.Additionally,according to the phase diagrams,the compound La2Fe14B was identified as a stable phase at high temperatures.It was found to be stable between 926.2 and 792.6℃;at low temperatures,however,it decomposed into α-La,α-Fe and LaFe_(4)B_(4),according to the reaction La_(2)Fe_(14)B→α-Fe+α-La+LaFe_(4)B_(4).

Collins Model and Phase Diagram of 2D Ternary System

The Collins model is introduced into the two-dimensional (2D) alternative ternary system having the Lennard-Jones (L-J) potential. The Gibbs free energy of this ternary system is calculated, and according to thermodynamic theory, a group of equations that determine the solid-liquid diagram of ternary system are derived, someisothermal sectional diagrams of the 2D ternary system are obtained. The results are quite similar to the behavior ofthree-dimensional substances.

A critical assessment of the roles of water molecules and solvated ions in acid-base-catalyzed reactions at solid-water interfaces

Solid-aqueous interfaces and phenomena occurring at those interfaces are ubiquitously found in a plethora of chemical systems.When it comes to heterogeneous catalysis,however,our understanding of chemical transformations at solid-aqueous interfaces is relatively limited and primitive.This review phenomenologically describes a selection of water-engendered effects on the catalytic behavior for several prototypical acid-base-catalyzed reactions over solid catalysts,and critically assesses the general and special roles of water molecules,structural moieties derived from water,and ionic species that are dissolved in it,with an aim to extract novel concepts and principles that underpin heterogeneous acid-base catalysis in the aqueous phase.For alcohol dehydration catalyzed by solid Bronsted acids,rate inhibition by water is most typically related to the decrease in the acid strength and/or the preferential solvation of adsorbed species over the transition state as water molecules progressively solvate the acid site and form extended networks wherein protons are mobilized.Water also inhibits dehydration kinetics over most Lewis acid-base catalysts by competitive adsorption,but a few scattered reports reveal substantial rate enhancements due to the conversion of Lewis acid sites to Brønsted acid sites with higher catalytic activities upon the introduction of water.For aldol condensation on catalysts exposing Lewis acid-base pairs,the addition of water is generally observed to enhance the rate when C–C coupling is rate-limiting,but may result in rate inhibition by site-blocking when the initial unimolecular deprotonation is rate-limiting.Water can also promote aldol condensation on Brønsted acidic catalysts by facilitating inter-site communication between acid sites through hydrogen-bonding interactions.For metallozeolite-catalyzed sugar isomerization in aqueous media,the nucleation and networking of intrapore waters regulated by hydrophilic entities causes characteristic enthalpy-entropy tradeoffs as these water moieties interact with kinetically relevant hydride transfer transition states.The discussed examples collectively highlight the utmost importance of hydrogen-bonding interactions and ionization of covalently bonded surface moieties as the main factors underlying the uniqueness of water-mediated interfacial acid-base chemistries and the associated solvation effects in the aqueous phase or in the presence of water.A perspective is also provided for future research in this vibrant field.

State of Pepsin and Acidic Protease in Solid Phase System and the Factors Increasing Their Destabilization

The adsorption state and catalytic properties of pepsin and acidic protease from microorganisms Asp. awamori and Asp. oryzae were studied in solid phase system （in presence of sorsilen, DEAE- and CM-cellulose）. According to the results, adsorption capacity and catalytic activity of enzymes depend on the physical nature of surface groups of the solid phase. Changing the stability of enzymes in the system with solid phase is observed even the adsorption bond is less stable （in the case of DEAE- and CM-cellulose in acidic media）. Injection to the medium ethanol, surfactants, sodium chloride and changing the temperature of the incubation medium could prevent the negative effects of the solid phases. When sorsilen is used as solid phase, pepsin and acidic protease from Asp. awamori suffer from high surface inactivation. Various surfactants influence adsorption state of enzymes differently. Non-ionic surfactants （Triton X-100） prevent adsorption and restore catalytic properties of enzymes.

A study revealing the key aroma compounds of steamed bread made by Chinese traditional sourdough

Aroma of Chinese steamed bread（CSB） is one of the important parameters that determines the overall quality attributes and consumer acceptance. However, the aroma profile of CSB still remains poorly understood, mainly because of relying on only a single method for aroma extraction in previous studies. Therefore, the objective of this study was to determine the volatile aroma compounds of five different samples of CSB using three different aroma extraction methods, namely solid-phase microextraction（SPME）, simultaneous distillation–extraction（SDE）, and purge and trap（PT）. All samples showed a unique aroma profile, which could be attributed to their unique microbial consortia.（E）-2-Nonenal and（E,E）-2,4-decadienal were the most prevalent aromatic compounds revealed by SDE, which have not been reported previously, while ethanol and acetic acid proved to be the most dominant compounds by both SPME and PT. Our approach of combining three different aroma extraction methods provided better insights into the aroma profile of CSB, which had remained largely unknown in previous studies.

Polarization of terahertz emission out of incident plane from laser interactions with solid targets

A powerful terahertz(THz) pulse was produced by a p-polarized,70 fs,800 nm laser interacting with solid targets at an incident angle of 45°.The polarization of the THz emission was measured out of the laser incident plane.The results showed that it was linearly polarized.We established a surface current model to explain this phenomenon,assuming that the transient current moving along the plasma surface was responsible for the generation of the THz emission.The model expectation and the experimental result were in good agreement.