Carbon-coated Fe₃O₄ (Fe₃O₄/C) microspheres activated with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC) were prepared, characterized and applied to adsorb bovine serum albumin (BSA). The prepared magnetic microspheres had spherical core-shell structure with a uniform and continuous carbon coating coupled with activation by EDC, and possessed superparamagnetic characteristics. The experimental results showed that the adsorption amount of BSA on the EDC-activated Fe₃O₄/C (Fe₃O₄/C-EDC) microspheres was higher than that on the Fe₃O₄/C microspheres. The maximum adsorption of BSA on Fe₃O₄/C-EDC microspheres occurred at pH 4.7, which was the isoelectric point of BSA. At low concentrations (below 1.0 M), salt had no noticeable effect on BSA adsorption. The BSA adsorption of Fe₃O₄/C-EDC microspheres had a better fit to the Langmuir model than the Freundlich isotherm and Temkin isotherm model, and the kinetic data were well described by the pseudo-second-order model. The adsorption equilibrium could be reached within 20 min. High desorption efficiency (97.6%) of BSA from Fe₃O₄/C-EDC microspheres was obtained with 0.5 M Na₂HPO₄ (pH 9.4) as the desorbent.

The Ni nanoparticles coated with Pb(Zr,Ti)O₃ (PZT) were synthesized by a sol-gel method and in situ reaction. And their structure, oxidation resistance, and electromagnetic properties were investigated. The X-ray diffraction patterns (XRD) exhibited that a small amount of impure phase characterized to Ni(OH)₂ was detected from the ammonia-treated Ni nanoparticles and the ammonia-treated Ni nanoparticles coated with PZT. After being pre-treated with aqueous ammonia, the PZT coating layer was more uniform and about 10 nm in thickness. The oxidation resistance of the ammonia-treated Ni nanoparticles coated with PZT, compared with that of the non-treated ones, was improved by about 66 °C. The PZT shell layer prepared by in-situ reaction can greatly reduce the dielectric constant and improve the natural resonance loss at high frequency, so as to obtain the optimal impedance matching performance of the electromagnetic wave transmission.

The elastic-plastic transition regime and brittle-ductile transition regime in scratch process for optical glass BK7 were analyzed based on the Hertzian equation and the stress ratio theory which was proposed by Wei. The interacting scratch process for optical glass BK7 with the grit interval distance as the variable was simulated by the ABAQUS software of finite element simulation based on the energy fracture theory. Double grits interacting scratch test for optical glass BK7 was carried out on the DMG ULTRASONIC 70-5 linear, by which the reliability of finite element simulation was verified. The surface morphology of the workpiece was analyzed by scanning electron microscopy (SEM), which showed that the width of groove increased obviously with the increase of scratch depth and the grit interval distance. Results of the width of groove were consistent with the simulation results. The subsurface damage layer was analyzed by the method of HF acid etching, which showed that there was an area of cracks intersecting. The scratching force was measured by the threedimensional dynamometer of KISTLER, which showed that the second scratching force increased with the increase of scratching depth and the grit interval distance. The force in the second scratch was smaller than that in the first time, which was consistent with the Griffith fracture theory.

Mesoporous La_0.8Sr_0.2MnO_3+σ/z SBA-15 (z = 1, 2, 4) perovskite oxides were synthesized via hard-templating with ordered mesoporous silica SBA-15 as the template. The as-prepared samples were characterized by XRD, SEM, AFM, BET, and XPS and the catalytic activity was tested for CO oxidation. The wide-angle XRD patterns showed that La_0.8Sr_0.2MnO_3+σ perovskite was formed. The SEM and AFM analyses exhibited that La_0.8Sr_0.2MnO_3+σ by hard-templating method had much smaller particle size (18 nm) than that (40 nm) by the sol-gel method. The perovskite-type oxides La_0.8Sr_0.2MnO_3+σ/z SBA-15 (z = 1, 2, 4) also displayed a higher BET surface area from 70 to 143.7 m²/g and a disordered mesostructure from nitrogen sorption analysis, as well as a small-angle XRD pattern. Moreover, the La_0.8Sr_0.2MnO_3+σ/z SBA-15 (z = 1, 2, 4) perovskite exhibited a much higher activity in CO oxidation than the conventional La_0.8Sr_0.2MnO_3+σ perovskite. Further analysis by the means of XPS techniques indicated that the existence of high content of O_ads/O_latt species contributed to the high activity.

A new appraisal method (QDA, quasi-distribution appraisal) which could be used to evaluate the finite element analysis of multi-functional structure made of honeycomb sandwich materials is developed based on sub-section Bezier curve. It is established by simulating the distribution histogram data obtained from the numerical finite element analysis values of a satellite component with sub-section Bezier curve. Being dealt with area normalization method, the simulation curve could be regarded as a kind of probability density function (PDF), its mathematical expectation and the variance could be used to evaluate the result of finite element analysis. Numerical experiments have indicated that the QDA method demonstrates the intrinsic characteristics of the finite element analysis of multi-functional structure made of honeycomb sandwich materials, as an appraisal method, it is effective and feasible.

The wetting behavior of Cu-Ti powder compacts with 22 wt % Ti and 50 wt % Ti on carbon materials, including graphite and carbon fiber reinforced carbon composites (CFC), has been investigated in a vacuum using the sessile drop method. The equilibrium contact angles of Cu-22Ti (containing 22 wt% Ti) on the graphite and the CFC substrates at 1 253 K are 32° and 26°, respectively, whereas the equilibrium contact angle of 9° is obtained for Cu-50Ti (containing 50 wt% Ti) on both the graphite and the CFC substrates at 1 303 K. Microstructural analysis of the wetting samples shows that a thin TiC reaction layer is developed at the interfacial area and Ti-Cu intermetallic compounds are formed over the reaction layer. The investigation on the spreading kinetics of Cu-Ti compacts on carbon materials substrates at fixed temperatures reveals that the spreading is controlled by the interfacial reactions in the first stage and then by the diffusion of the active Ti from the drop bulk to the triple line in the later stage. The spreading is promoted by the intense reaction at higher Ti concentrations.

TiC _x/Cu composites were fabricated by combustion synthesis and hot press technology. Using XRD, SEM, EDS, FESEM analysis methods, the effects of various carbon sources and different Cu contents on the microstructures of TiC _x/Cu composites and the size of TiC _x particles were investigated. Results showed that TiC _x reinforcing particles size increases with decreasing Cu content in Cu-Ti-C reaction system. With carbon nanotubes (carbon black) serving as carbon source, the generated TiC _x particles size transits from nanometer to submicron when Cu content corresponding to the reaction system is reduced to 60 vol% (70 vol%); while graphite serves as carbon source, there is no clear limiting concentration. C particles with smaller size, larger specific surface area and better distribution result in finer TiC _x particles, which is more beneficial to generating nano-sized TiC _x/Cu composites.

Slag glass melting is usually performed on a laboratory scale in crucibles, which are economically viable tools for the production of slag glass-ceramics. In this work, quaternary CaO-Al₂O₃-MgOSiO₂ (CAMS) glass-ceramics were prepared by melting the tailing of Bayan Obo mine tailing, blast furnace slag, and fly ash in alumina and graphite crucibles. The effect of the crucible material on the microstructure and properties of the glass-ceramics was investigated using differential scanning calorimetry, X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy and inductively coupled plasma atomic emission spectroscopy. Results indicated that the contents of Al₂O₃ and Fe₂O₃ in the initial glass were significantly changed by the corrosion of the alumina crucibles during the glass melting process and by the reducing action of the graphite crucibles. The main crystal phases of glass-ceramics melted in alumina crucibles and graphite crucibles were Ca (Mg, Fe, Al) (Si, Al)₂O₆, coesite and Ca (Mg, Al) (Si, Al)₂O₆, respectively. According to these findings, we conclude that the microstructure and properties of the glass-ceramics are affected by the crucibles.

The preparation of hydroxyl chromium oxide by hydrogen reduction of disodium chromate and particulate hydroxyl mechanical activation features were studied. Then with self-made hydroxyl chromium as the raw material, a direct reduction and carburization process was used to prepare ultra-fine chromium carbonization. Through SEM and XRD, the high performance mechanical activation, key coefficients, microstructure, hardness and wear-resisting property were investigated. The results reveal that suitable mechanical activation and carbon reducing carbonization temperature, carbonization time, carbon content are beneficial to obtaining ultra-fine chromium carbonization. Typically, when the time of high performance grinding is 5 min, the carbon reducing temperature is 1 100 ℃, the carbon reducing time is 1 h, the carbon content is 28%, and finally the particle size of chromium carbide powder is 1 μm. Under this condition of preparation of ultra-fine chromium carbide, both the hardness and wear resistance are better than those in the industrialization of chromium carbide coating.

Ferroelectric and leakage properties are important for ferroelectric applications. Pure and Nd-doped (x=0.05-0.20) BiFeO3 thin films were fabricated by sol-gel method on FTO substrates. The phase structure, surface morphology, leakage current, ferroelectric properties, and optical properties of BiFeO₃ ^- based thin films were investigated. The substitution of Nd³⁺ ions for the Bi3+ site converts the structure from rhombohedral to coexisting tetragonal and orthorhombic. Nd doping improves the crystallinity of BiFeO₃ thin films. The leakage current of Nd-doped BiFeO₃ decreases by two to three orders of magnitude compared with that of pure BiFeO₃. Among the samples, 15% Nd-doped BiFeO₃ exhibits the strongest ferroelectric polarization of 17.96 μC/cm². Furthermore, the absorption edges of Bi_1-xNd _xFeO₃ thin films show a slight red-shift after Nd doping.

The sintering of chromium-containing vanadium-titanium magnetite using different coke contents was studied through the sintering pot tests, X-ray diffraction analysis and mineralogical phase analysis. Results showed that, as the coke content increased from 3.2% to 4.4%, the liquid phase and combustion zone thickness increased while the vertical sintering rate and ratio of sintered product decreased. In addition, the combustion ratio of exhaust gas also increased with increasing the coke content, indicating that combustion zone temperature also increased, and the excessive the coke content in the sintering process of vanadiumtitanium magnetite is harmful. As the coke content increased, the magnetite, silicates, and perovskite contents of the sintered ore increased while the contents of hematite and calcium ferrite of sintered ore decreased; drum strength decreased, and reduction degradation properties increased while reduction ability decreased. We found that the appropriate coke content for the sintering process is 3.6 wt%.

α-MoO₃ nanobelts/carbon nanotubes (CNTs) composites were synthesized by simple hydrothermal method followed by CNTs incorporating, and characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Cyclic voltammogram (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge testing techniques were employed to evaluate the electrochemical behaviors of α-MoO₃ nanobelts /CNTs composites. The results exhibited that compared to bare α-MoO₃ nanobelts, the α-MoO₃ nanobelts/CNTs composites have better electrochemical performances as cathode materials for lithium ion battery, maintaining a reversible specific capacity of 222.2 mAh/g at 0.3 C after 50 cycles, and 74.1% retention of the first reversible capacity. In addition, the Rct value of the α-MoO₃ nanobelts/ CNTs is 13 Ω, much lower than 66 Ω of the bare α-MoO₃ nanobelts. The better electrochemical performances of the α-MoO₃ nanobelts /CNTs composites can be attributed to the effects of the high conductive CNTs network.

A series of CdS with various shapes of microsphere, flower-like and leaf-like were templatefreely synthesized by a hydrothermal method. Powder X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM) and UV-vis absorption spectroscopy (UV-vis) were applied to characterize the morphology, optical and other physical properties of the as-prepared CdS. An optical spectrum analyzer was used to measure the wavelength of the illuminant on the slurry in the activity evaluations of photocatalytic reduction of CO₂ over CdS. Both sources of cadmium and sulfur had great impact on the CdS morphology as can be seen in the SEM images. By means of a series of activity evaluations, the microspheric CdS made from cadmium nitrate and thioacetamide showed better photocatalytic activity for the reduction of CO₂ to methyl formate (MF) in methanol than the flower-like and leaf-like CdS catalysts.

The effect of heterogeneous Fenton reaction was studied on methylene blue (MB) and Nitrosomonas europaea (N. europaea) cells. Four Fenton systems were prepared and compared with each other, including Nickel Foam (NF)/TiO₂, NF/Bi₂WO₆, Ceramic foam (CM)/TiO₂, and CM/Bi₂WO₆. The order of effect of fenton reaction ranked as NF/TiO₂>CM/TiO₂>NF/Bi₂WO₆>CM/Bi₂WO₆. In acid or alkaline solution, the removal efficiency also decreased compared with neutral solution. With lower pH values, the nanoparticles were easier to break off from NF skeleton. Thus the synergetic effect of photocatalysis and fenton reaction can not take action. As for CM skeleton, the bond–Si-O-can bind with TiO₂ or Bi₂WO₆. The membrane fluidity was used as an indicating parameter. After being treated by Fenton reaction, N. europaea surface was rougher than the native bacterium and the bulges on cell surface became irregular, which is attributed to change of lipopolysaccharide patches. Polarization of N. europaea cell membrane in acid medium increased more obvious than alkaline medium.

The visible-light-active mesoporous cuprous oxide nanoparticles were successfully synthesized via a facile precipitation process with the presence of gelatin, which was demonstrated to play an important role in the formation of mesoporous structure and the grain size control. The nanoscale grain size and mesoporous structure lead to lager specific surface area with the addition of gelatin. Furthermore, the photodegradation of as-prepared catalysts in the presence of gelatin toward the negatively charged methyl orange (MO) was investigated. The cuprous oxide displayed an excellent visible light photocatalytic activity of MO, owing to its exposed active (111) face and large specific surface area. The adsorption of positively charged methyl blue (MB) revealed that the mesoporous cuprous oxide displayed better adsorption of anionic dye MB due to the residual gelatin on the surface of the grains, compared to that in the absence of gelatin.

To improve the cyclic stability at high temperature and thermal stability, the spherical Al₂O₃-modified Li(Ni_0.5Co_0.2Mn_0.3)O₂ was synthesized by a modified co-precipitation method, and the physical and electrochemical properties were studied. The TEM images showed that Li(Ni_0.5Co_0.2Mn_0.3)O₂ was modified successfully with nano-Al₂O₃. The discharge capacity retention of Al₂O₃-modified Li(Ni_0.5Co_0.2Mn_0.3)O₂ maintained about 99% after 200 cycles at high temperature (55 °C), while that of the bare one was only 86%. Also, unlike bare Li(Ni_0.5Co_0.2Mn_0.3)O₂, the Al₂O₃-modified material cathode exhibited good thermal stability.

The effect of multi-walled carbon nanotubes (MWCNTs) on the mechanical properties and microstructure of sulfur aluminate cement (SAC) composites was investigated. The dispersed MWCNTs were added into SAC in various weight contents.The results of mechanical properties of the MWCNTs/SAC composites indicated that the addition of 0.08 wt% MWCNTs can improve the SAC compressive strength, flexural strength, and bend-press ratio by 15.54%, 52.38%, and 31.30% at maximum, respectively. The degree of SAC hydration and porosity and pore size distribution of the matrix were measured by X-ray diffraction (XRD), thermal analysis (TG/DTG), and mercury intrusion porosimetry (MIP). Results show that the addition of MWCNTs in SAC composites can promote the hydration of SAC and the formation of C-S-H gel, reduce the porosity and refine the pore size distribution of the matrix. The microstructure was characterized by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). It is found that the MWCNTs have been dispersed homogeneously between the hydration products of SAC paste and act as bridges and networks between cracks and voids, which prevents the development of the cracks and transfers the load.

The microstructural study was conducted on cement and cement-slag pastes immersed in different concentrations of Mg(NO₃)₂ solutions utilizing ²⁹Si, ²⁷Al NMR spectroscopy and XRD techniques. The results show that the hydration of both the cement and cement-slag pastes is delayed when the pastes are cured in Mg(NO₃)₂ solutions as compared to the pastes cured in water. Moreover, Mg²⁺ ions also exhibit an decalcifying and dealuminizing effect on the C-A-S-H in cement and cement-slag pastes, and thereby decrease Ca/Si and Al[4]/Si ratios of the C-A-S-H. The dealuminization of C-A-S-H is mitigated for cement-slag paste as compared to pure cement paste. The depolymerized calcium and aluminum ions from C-A-S-H gel mainly enter the pore solution to maintain the pH value and form Al^[6] in TAH, respectively. On the other hand, Mg²⁺ ions exert an impact on the intra-transition between Al^[6] species, from AFm and hydrogarnet to hydrotalcite-like phase. NO₃ ^- ions are interstratified in the layered Mg-Al structure and formed nitrated hydrotalcite-like phase (Mg_1-xAl _x(OH)₂(NO₃) _x•nH₂O). Results from both ²⁷Al NMR and XRD data show that ettringite seems not to react with Mg²⁺ ions.

We experimentally studied the fine lightweight aggregate with the particle size range of 3.15-4.75 mm used as functional bridge between FRP sheet and concrete substrate. However, problems would appear and how to deal with the interfacial transition zone (ITZ) and make it stronger is the key point for this concept. Considering that silane coupling agent (SCA) can provide a better bond on a silicon-containing material surface, it was introduced as a modifying material to further improve the bond quality of the ITZ between lightweight aggregate and cement paste. Results indicated that the water absorptivity of lightweight aggregate can be controlled by SCA solutions, and the pull-off bond strength, mechanical strength, and microhardness were increased, which was attributed to the optimized microstructure under the condition of an appropriate concentration of SCA.

The relationship between compressive strength obtained by universal testing machine and rebound value obtained by the hammer of high performance concrete was systematically investigated at the macro level. And a model of high performance concrete strength curve was established from them. At the micro level, the microstructure, hydration products and pore structure of concrete surface were analyzed by scanning electron microscopy (SEM), comprehensive thermal analysis (TG-DSC) and mercury intrusion porosimetry (MIP), respectively. The effect of carbonation on surface strength was also investigated. The results showed that the concrete surface hardness layer grew rapidly at early stage and then stabilized at last with ongoing curing age; the rebound value and compressive strength of concrete with slag were higher than those of concrete with the same content of fly ash. In addition, the strength curve obtained by the least square method can satisfy the local standard requirements with an average relative error of 8.9% and a relative standard deviation of 11.3%. When the carbonation depth was 6 mm, the compressive strength calculated by national uniform strength curve was 25 PMa higher than that by high performance concrete.

Electromagnetic (EM) wave absorbing cement-based composite has promising applications in protecting civil and military buildings from electromagnetic interferences. A new idea of preparing EM wave absorbing cement-based composite is proposed by using ceramsite containing iron oxide as EM wave absorbing functional aggregate. The ceramsite was synthesized by adding 10 wt% Fe₃O₄ into clay and sintering at 1 200 °C, which shows obvious dielectric and magnetic loss properties for electromagnetic wave. The maximum reflection loss (RL) of the concrete specimens prepared with the ceramsite is between -10.2—10.7 dB (corresponding to absorption greater than 90% EM energy) in the bandwidth of 8-18 GHz. In addition, the compressive strength at 28 days age of the concrete is 46 MPa, showing the potentiality of being used as structural components in buildings.

Fly ash cenospheres (FACs) as a recycling material of industrial waste has become a competitor for other inorganic particle fillers. Epoxy resin (EP) composites reinforced with different content of FACs as well as different size grading ratio were prepared. The surface modification of FACs particles was conducted before incorporating into EP matrix. The impact and flexural strengths and the flexural modulus were investigated, and the fracture surfaces of the testing samples were analyzed using SEM. Results showed that FACs had an obvious effect on the mechanical characteristics of the FACs/EP composites. With increasing weight fraction of FACs, the impact and flexural strengths and the flexural modulus of EP composite samples increased, and reached the highest values when the weight fraction of FACs reached 15 wt%. The mechanical characteristics of the FACs/EP composites however deteriorated with further increasing of FACs content. For the EP composites reinforced with different size grading ratio of FACs, the larger proportion of small FACs particles, the better mechanical properties of the EP composites. The results were analyzed from the aspect of the plastic deformation, new surface formation and fracture absorption energy. The synergistic effect of the size grading ratio of FACs was not obvious, which would be further investigated.

In order to determine a proper compaction temperature that affects the workability and compactibility of the polymer-modified asphalt (PMA), the effect of compaction temperature was examined on the volumetric properties and the compaction energy indices. Change in compaction temperature shows an important influence on the maximum specific gravity of mixture (G _mm) by internal volume change of PMA. The change in G _mm mainly affects the effective volume of the aggregate (V _Eff). Reduction in V _Eff from Zero shear viscosity (ZSV) to superpave temperature allows 0.1%-0.15% of the asphalt binder to occupy highly the external voids of aggregates. The volumetric properties for all compaction specimens meet superpave criteria, but the energy efforts were the lowest at ZSV temperature. Lower energy efforts at the ZSV temperature reflect easier compaction than those at excessively high temperature. Clearly, excessive compaction temperature may not be necessary to improve the compactibility and to reduce the compaction efforts.

The performances of the cement-based materials can be improved by the incorporation of polypropylene fiber, but the damage processes become more complex with different fiber contents at the same time. The acoustic emission (AE) technology can achieve the global monitoring of internal damage in materials. The evolution process of failure mode and damage degree of polypropylene fiber reinforced mortar and concrete were analyzed by measuring the AE energy, RA value, AF value and b value. It was found that the cement matrix cracked on the initial stage, the cracks further developed on the medium stage and the fibers were pulled out on the last stage. The matrix cracked with minor injury cracks, but the fiber broke with serious damage cracks. The cumulative AE energy was proportional to the polypropylene fiber reinforced concrete and mortar’s ductility. The damage mode and damage degree can be judged by identifying the damage stage obtained by the analysis of the AF value.

To improve the mechanical properties of alumina particulates reinforced steel matrix composite, Ti powder was added into the alumina preform, a 5140 steel matrix composite was fabricated by squeeze casting, and the influences of Ti powder on the microstructure, hardness and bending strength of the composite were investigated, compared with the composite without adding Ti powder. Applied Ti powder and alumina particulates were 10-25 μm and 100-180 μm in size, respectively. Both composites were successfully fabricated, however Ti powder addition increased the infiltration thickness of the composite. In the Ti contained composite, a TiC film in micron scale is formed on the surface of alumina particles, many TiC aggregates are dispersed in the steel matrix without obvious remaining Ti powder. The hardness and the three-point bending strength of the composite reach 49.5 HRC and 1 018 MPa, respectively, which are 17.9% and 52.4% higher than those of the composite in the absence of Ti addition. Fracture morphology shows that the debonding of alumina particulates is eliminated for the composite in the presence of Ti addition. Sessile drop test shows the average wetting angle between 5140 steel and that of Ti coated Al₂O₃ is about 82.15°, much lower than the wetting angle 150° between steel and pure Al₂O₃. Therefore, the increase in the mechanical properties of the composite is attributed to the improvement of Al₂O₃p/steel interface wetting and bonding by adding Ti powder in the preform.

SiC/Gr/ZL101 aluminum-based composites were prepared by semi-solid stirring and gravity pouring method. The effects of SiC/Gr with different volume fractions on the microstructure and property of aluminum-based composites were studied by means of microstructure observation, tensile test, fracture scanning analysis and damping capacity test. The results show that the primary phase α-Al of ZL101 alloy prepared by semi-solid stirring and gravity pouring method is fragmented dendrite, along with the rising SiC volume fractions, the tensile strength of the composites first increases and then decreases while its elongation gradually decreases, the maximum tensile strength of the material can reach 168 MPa, up to 16% than that of ZL101 alloy, the fracture morphology is obviously brittle fracture. They also show that the addition of SiC and Gr improves the damping capacity of ZL101 alloy, the internal dissipation Q ^-1 of the composites is obviously higher than that of matrix alloy and gradually increases along with the rising SiC volume fractions. The damping mechanism of the composites is mainly the combined effects of both dislocation damping and interfacial damping.

The high strength bridge steel was processed with the simulated coarse grain heat affected zone (CGHAZ) thermal cycle with heat input varying from 30 to 60 kJ/cm, the microstructures were investigated by means of optical microscope (OM), scanning electron microscope (SEM), electron backscattering diffraction (EBSD) and transmission electron microscope (TEM), and the impact properties were evaluated from the welding thermal cycle treated samples. The results indicate that the microstructure is primarily composed of lath bainite. With decreasing heat input, both bainite packet and block are significantly refined, and the toughness has an increasing tendency due to the grain refinement. The fracture surfaces all present cleavage or fracture for the samples with different heat inputs. Moreover, the average cleavage facet size for the CGHAZ is nearly equal to the average bainite packet size and the bainitic packet boundary can strongly impede the crack propagation, indicating that the bainitic packet is the most effective unit in control of impact toughness in the simulated CGHAZ of high strength bridge steel.

The Cu-15Cr in-situ fiber-reinforced composites sheets were prepared by cold drawing combined with cold rolling process. The evolution process of Cr fibers was studied, and when cold rolling reduction ε = 95%, the morphology of Cr fiber at different annealing temperature and the thermal stability of Cu-15Cr alloy were studied. Microstructure was also studied by scanning electron microscopy (SEM). Meanwhile, the tensile strength of the alloy was tested by means of a precision universal tester, and the resistance value of the alloy was determined by using a digital micro-Euclidean instrument. The experimental results show that, with the increase of deformation, Cr dendrites evolve into homogeneous and parallelly arranged Cr fibers, and the cross-section of Cr fibers undergoes a "V" shape transition to "一" shape. In addition, spheroidization of the Cr fibers occurs on edges and extends to the center as annealing temperature rises. Moreover, the Cr fibers remains stable when the annealing temperature is below 550 °C. Furthermore, the tensile strength of Cu-15Cr alloy decreases gradually as the annealing temperature increases, while the electrical conductivity maximizes when annealing at 550 °C. Our study also shows that Cu-15Cr alloy has obtained a better comprehensive performance with tensile strength of 656 MPa and electrical conductivity of 82%IACS after annealing at 450 °C.

The impact of rare earth element La on the microstructure and hot crack resistance of ADC12 alloy was analyzed. The additive amount of La was 0%, 0.3 wt%, 0.6 wt% and 0.9 wt%, respectively. The results showed that, with the increase of the additive amount from 0% to 0.6 wt%, the grain shape of α-Al gradually varied from developed dendritic crystal into fine dendritic crystal, equiaxed crystal and spheroidal crystal; eutectic silicon varied from needle-like or tabular shape into fine rod like shape; the hot crack force of the alloy also gradually decreased. However, when the additive amount of La reached 0.9 wt%, the excessive amount of rare earth elements was segregated within grain boundary area, forming intermetallic compounds. Therefore, the grain size of α-Al, eutectic silicon and the hot crack force of the alloy all increased. In the case that the additive amount of La reached 0.6 wt%, the best metamorphism effect and most excellent hot cracking resistance capacity of alloy were presented. The poisoning effect of rare earth element on eutectic silicon and the constitutional supercooling caused by rare earth element were the major causes for alloy modification, alloy refinement, and the main reasons for the increased hot cracking resistance.

First-principles calculations have been carried out to investigate the effects of alloying elements (Zn, Li, Y and Sc) on the electronic structure, elastic and thermal properties of Mg solid solution. The calculated cohesive energies show that Mg-Sc has the highest structural stability. The calculations of the densities of states (DOS) and electronic charge density difference indicate that Mg-Y (Sc) alloys have very strong covalent bonding due to a very strong Mg p-Y(Sc) d hybridization. The bulk modulus B, shear modulus G, Young's modulus E and Poisson ratio ν are derived using Voigt-Reuss-Hill (VRH) approximation. The results show that all the alloys can exhibit ductile properties at 2.77 at% R, and Mg-Zn(Li) alloys have the better ductility and plasticity. In the end, the Debye temperature and isochoric heat capacity are also calculated and discussed.

Electropulsing is introduced into the cutting process for quenched and tempered 45 steel, which is a novel method to improve the material machinability compared with the conventional cutting process. The effects of electropulsing on cutting performances, microstructure evolution, and surface qualities of 45 steel rods were studied. The results indicate that electropulsing is beneficial for the cutting process in 3 aspects as follows: (1) reducing the principal cutting force, surface microhardness and surface roughness of the machined sample dramatically; (2) improving the machining efficiency and prolonging the life of cutting tools; (3) decreasing the thickness of rheological layer which was usually caused by work hardening in the cutting process. The morphology and microstructure of the cutting chips showed that the length of the chips increased significantly with the increase of the current density. The advantage of electropulsing is that it can improve the plastic deformation capability as well as increase the lubricating property between the specimen and the cutting tool.

Novel organic-inorganic composites were in-situ synthesized by using TriSilanolPhenyl polyhedral oligomeric silsesquioxane (SO-POSS) as fillers and poly(2,5-benzimidazole) (ABPBI) as polymer matrix. The uniformly dispersed 3% SO-POSS particles in ABPBI matrix increased the thermal stability of the composite membranes. It was found that both the water and H₃PO₄ uptakes were increased significantly with the addition of SO-POSS due to the formation of hydrogen bonds between the POSS and H₂O/H₃PO₄, which played a critical role in the improvement of the conductivity of the composite membranes at temperature over 100 °C. Proton conductivities of H₃PO₄ doped with 3wt% SO-POSS contained ABPBI membranes increased with the increase of H₃PO₄ absorbance, reaching the maximum proton conductivity of 2.55 × 10^-3 S·cm^-1 at 160 °C, indicating that the ABPBI/SO-POSS composite membrane could be a promising candidate for mid-temperature PEMFCs.

Diblock copolymers polystyrene-block-polyvinyltriethoxysilane (PS-b-PVTES) were synthesized via atom transfer radical polymerization (ATRP), which self-assembled into spherical micelles in solvent of THF-methanol mixtures. The self-assembled micelles were immobilized by cross-linking reaction of VTES in a shell layer of micelles. The chemical structures of block copolymers and morphology of micelles were characterized in detail. It was found that the size of immobilized micelles was strongly affected by the copolymer concentration, composition of mixture solvent, and block ratios.

The dispersion ability of polycarboxylate superplasticizer (PCE) in fresh concrete was much impeded by clay impurities. To improve the dispersion of PCE in the clay-contained concrete, a novel PCE with carboxyl as a specific branched chain terminal group was synthesized, using modified polyether as the raw material which was prepared through esterification between hexahydrophthalic anhydride (HHPA) and isobutenyl polyoxyethylene ether (IPEG) with hydroxy as the terminal group. The esterification product and PCE molecular structure were characterized by infrared spectroscopy and 1HNMR resonance. The results confirmed that the product molecular structure was a comb-type copolymer with long-chain terminal carboxyl group and PEO attached directly to the backbone chain. The as-synthesized PCEs had favorable dispersibility in cement than conventional PCE in the presence of montmorillonite (Mmt) clay. This can be attributed to the introduction of electronegative carboxyl to PCE long-chain terminal group, which reduces the adsorption of PCE on Mmt, and thus improves the tolerance of PCE to the Mmt.

In order to prepare hydrophobic waterborne polyurethane coatings with better performances, the silicon-containing waterborne polyurethane (SiWPU) with functional chain extender hydroxyethyl acrylate (HEA) was prepared first, and then a series of silicon&fluorine-containing polyurethane/acrylate (FSiPUA) emulsions were obtained with flourine containing acrylic monomer by seed emulsion polymerization, introducing micro-nano SiO₂ into FSiPUA emulsion to make the final hybrid emulsion. The properties of SiWPU, FSiPUA and SiO₂/FSiPUA were investigated by fourier transform infrared spectra (FTIR), transmission electron microscope (TEM), Scanning Electron Microscope (SEM) and some other analytical methods. The results revealed that FSiPUA emulsion particles possessed composite core-shell structure and FSiPUA films with suitable ratio performed better than SiWPU films in hardness, water resistance and solvent resistance. The SiO₂/FSiPUA films with micro-nano dual roughness structure showed a water contact angle of 136° with good resistance to acid and alkali.

A hot-press tackified preform was used to improve the uniformity of the laminates thickness and the mechanical properties of the obtained laminates were studied using vacuum assisted resin transfer molding (VARTM). Two modified preforms were prepared under 0.1 and 0.6 MPa in an autoclave and then were used to fabricate the laminates via VARTM. Permeability and thickness distribution of the laminates were obtained by using a special device. Moreover, the tensile and compressive strengths of the obtained laminates were studied and compared with the unmodified ones. Results show that the tackified laminates present a maximum and minimum thickness under 0.1 and 0.6 MPa, respectively. The thicknesses and in-plane permeability of the tackified laminates, with better thickness uniformity, are significantly decreased compared with that of the unmodified cases, while the tensile and compressive strengths of the tackified laminates are improved obviously. Results show that the mechanical property of the tackified laminates prepared by hotpressing at 0.1 MPa is better than that processed at 0.6 MPa.

L-(+)-α-(positive butyl)-leucine ethyl ester bromide chiral ionic liquid was synthesized by using microwave-assisted synthesis method and L-(+)-α-(positive butyl)-leucine ethyl ester terafluoroborate and hexafluorophosphate chiral ionic liquids were synthesized by the anion exchange reaction. The structures were characterized by IR, 1HNMR and structure optimization calculation. The results of studies on physicochemical properties show that they possess better thermal stability, solubility, bio-solubility and high conductivity. They can serve as effective reaction media as well as chiral catalysts. They are presently being investigated as dispersion agents in molecular imprinting ployer.

Magnetic fluorescent dual-drug nanocomposites (MFDDs) were developed with the aim of simultaneouly delivering two different anticancer drugs, kaempferol (KAE) and paclitaxel (PTX). Firstly, Fe3O4/ bovine serum albumin (Fe₃O₄/BSA) composite microspheres with physically entrapped KAE were prepared, then microspheres were modified with PTX/graphene quantum dots (PTX/GQDs) through chemically bonding, and the MFDDs were obtained. The properties of nancomposites were characterized by X-ray diffractometry, Fourier-transform infrared spectroscopy, transmission electron microscopy, vibrating sample magnetometry and X-ray fluorescence spectrometry. It was found that the superparamagnetic nanocomposites had ultrafine size (below 110 nm), high saturation magnetization of 24.36 emu/g, and significant fluorescence. Furthermore, the cumulative in vitro release of the MFDDs exhibited controlled drug release. Cell viability experiments confirmed that the co-administration of KAE with PTX had a superior cytotoxicity to the Hela cells compared with single drug-loaded forms. Therefore, dual anticancer drug-loaded MFDDs have the potential to be used for cancer combined chemotherapy.