Preparation of High Performance Foamed Concrete from Cement,Sand and Mineral Admixtures

The titled high performance foamed concrete was developed from Portland cement, ultra fine granulated blast-furnace slag, pulverized fly ash and condensed silica fume by means of pre-foaming process. The resultant foamed concrete presents its thermal conductivity of about 0.16-0.75 W/（m·℃） and 28 d compressive strength of about 1.1-23.7 MPa when its mix proportion varies in the range of cement content 280 kg-650 kg/m^3, fly ash 42-97 kg/m^3, slag 64-146 kg/m^3, silica fume 34-78 kg/m^3, and sand 0-920 kg/m^3. The compressive strength of the foamed concrete with oven dried bulk density of 1500 kg/m^3 in appropriate mix proportion and with small amount of superplasticizer reached as high as 44.1 MPa. Meanwhile, the flesh foamed concrete behaves like an excellent flow-ability, therefore, is especially suitable for the application in case of massive foamed concrete casting in situ and in the case of filling casting into large volume underground irregular voids, except for pre-casting of building components like blocks, bricks, and wall panels.

Physical Modeling of the Vacuum Circulation Refining Process of Molten Steel

The available studies in the literature on physical modeling of the vacuum circulation (RH, i.e. Ruhrstahl Heraeus) refining process of molten steel have briefly been reviewed. The latest advances made by the author with his research group have been summarized. Water modeling was employed to investigate the flow and mixing characteristics of molten steel under the RH and RH KTB (Kawasaki top blowing) conditions and the mass transfer features between molten steel and powder particles in the RH PTB (powder top blowing) refining. The geometric similarity ratio between the model and its prototype (a multifunction RH degasser of 90 t capacity) was 1:5. The effects of the related technological and structural factors were considered. These latest studies have revealed the flow and mixing characteristics of molten steel and the mass transfer features between molten steel and powder particles in these processes, and have provided a better understanding of the refining processes of molten steel.

Strength Development and Microstructure of Hardened Cement Paste Blended with Red Mud

Red mud was activated to be a mineral admixture for Portland cement by means of heating at different elevated temperatures from 400 ℃ to 700 ℃ . Results show that heating was ef-fective, among which thermal activation of red mud at 600 ℃ was most effective. Chemical analysis suggested that cement added with 600 ℃ thermally activated red mud yielded more calcium ion dur-ing the early stage of hydration and less at later stage in liquid phase of cement water suspension sys-tem, more combined water and less calcium hydroxide in its hardened cement paste. MIP measure-ment and SEM observation proved that the hardened cement paste had a similar total porosity and a less portion of large size pores hence a denser microstructure compared with that added with original red mud.

Geochemical Characteristics of Cenozoic Basaltic High-K Volcanic Rocks from Maguan Area, Eastern Tibet

The major element, trace element and Nd-Sr isotopic composition of Cenozoic basaltic volcanic rocks from the Maguan area, eastern Tibet, indicates that the volcanic rocks are enriched in alkalis, especially K (K-2O up to {3.81%}) and depleted in Ti (TiO-2={1.27%}-{2.00%}). These rocks may be classified as two groups, based on their Mg+# numbers: one may represent primary magma (Mg+# numbers from 68 to 69), and the other, the evolved magma (Mg+# numbers from 49 to 57). Their REE contents are very high (∑REE={155.06}-{239.04}μg/g). Their REE distribution patterns are of the right-inclined type, characterized by LREE enrichment [(La/Yb)-N={12.0}-{19.2}], no Ce anomaly (Ce/Ce+*={1.0}), and weak negative Eu anomaly (Eu/Eu+*={0.9}). The rocks are highly enriched in Rb, Sr and Ba ({59.5}-{93.8} μg/g, 732-999 μg/g, and 450-632 μg/g, respectively), high in U and Th ({1.59}-{2.31} μg/g and {4.73}-{8.16} μg/g, respectively), and high in Nb, Ta, Zr and Hf (70-118 μg/g, {3.72}-{5.93} μg/g, 215-381 μg/g, and {5.47}-{9.03} μg/g, respectively). In the primitive mantle-normalized incompatible element spidergram, Nb, Ta, Zr, Hf and P show positive anomalies, whereas Ba, Ti and Y show negative anomalies. The {{}+{87}Sr/+{86}Sr} ratios range from {0.704029} to {0.704761}; {{}+{143}Nd/+{144}Nd} from {0.512769} to {0.512949}; and εNd from {+2.6} to {+6.1}. These geochemical features might suggest that the potential source of the basaltic high-K volcanic rocks in the Maguan area is similar to the OIB-source mantle of Hawaii and Kergeulen volcanic rocks.

Influential Factors on Deicing Performance of Electrically Conductive Concrete Pavement

The deicing experiment of carbon fiber reinforced electrically conductive concrete （CFRC） slab was conducted in laboratory at first, then the deicing process of CFRC parement was analyzed by means of finite element method （FEM）. At last, based on the energy conservation law and the computing restdts of finite element method, the influential factors including the setting of electric heating layer, environmental temperature, the thickness of ice, material parameters, and deicing power on deicing performance and energy consumption were discussed.

Kinetics of Liquid-Phase Hydrogenation of Toluene Catalyzed by Hydrogen Storage Alloy MlNi_5

The kinetics of liquid-phase hydrogenation of toluene catalyzed by MlNi_5 was studied by investigating the influences of the reaction temperature and pressure on the mass transfer-reaction processes inside the slurry. The results show that the reaction rate accelerates when the reaction temperature increases, and reaches its maximum at about 490 K, but if temperature is higher than 510 K, the reaction rate decreases rapidly. The whole reaction process is controlled by the reaction at the surface of the catalyst particles. The mass transfer resistance at gas-liquid interface and that from the bulk liquid phase to the surface of the catalyst particle can be neglected. The apparent reaction rate is zero order for toluene concentration and first order for hydrogen concentration in the liquid phase. The kinetic model is obtained. The kinetic model fits the experimental data very well. The apparent activation energy of the hydrogen absorption reaction of MlNi_5-toluene slurry system is 41.01 kJ·mol^(-1).

Flow stress and softening behavior of wrought magnesium alloy AZ31B at elevated temperature

The flow stress and softening behavior of AZ31B magnesium alloy in hot compression were investigated. The relationship of flow stress, temperature and strain rate was appropriately described with the exponential form of Zener Hollemen parameter during steady state deformation of alloy at 573723 K, 0.015s -1 . Dynamic recrystallization is the softening mechanism of AZ31B in hot compression. The flow curves of alloy have almost no peak value at 723 K and lower strain rate, presenting feature of geometric dynamic recrystallization.

Development of liquid-nitrogen-cooling friction stir spot welding for AZ31 magnesium alloy joints

A liquid-nitrogen-cooling friction stir spot welding(C-FSSW) technology was developed for welding AZ31 magnesium alloy sheets. The liquid-nitrogen cooling degraded the deformability of the welded materials such that the width of interfacial cracks increased with increasing cooling time. The grain size of the stirred zone(SZ) and the heat-affected zone(HAZ) of the C-FSSW-welded joints decreased, whereas that of the thermomechanically affected zone(TMAZ) increased with increasing cooling time. The maximum tensile shear load of the C-FSSW-welded joints welded with a cooling time of 5 or 7 s was larger than that of the friction stir spot welding(FSSW)-welded joint, and the tensile shear load decreased with increasing cooling time. The microhardness of the C-FSSW-welded joints was greater than that of the FSSW-welded joint. Moreover, the microhardness of the SZ and the HAZ of the C-FSSW-welded joints increased, whereas that of the TMAZ decreased, with increasing cooling time.

Formation of Aluminum-magnesium Alloy Cup by Hydrodynamic Deep Drawing with Twin-loading Paths

In order to overcome the limitation of hydro-rim deep drawing, a new process of hydrodynamic deep drawing （HDD） with independent radial hydraulic pressure was proposed. By employing the dynamic explicit analytical software ETA/DynaformS.5 which is based on LS-DYNA3D, the effects of independent radia! hydraulic pressure on the stress, strain and the sheet-thickness of aluminum-magnesium cylindrical cup with a hemispherical bottom were analyzed by numerical simulation. The feature of stress distribution is that there exists a stress-dividing circle in the flange, and the radius of dividing circle was determined by theoretical analysis and stimulation. The experimental results indicate that the reasonable match of independent radial hydraulic pressure and liquid chamber pressure can effectively reduce the thinning at the bottom of hemisphere, decrease the radial stress-strain, and improve the drawing limit of aiuminum-magnesium alloy cylindrical cup.

Shrinkage Behavior of High Performance Concrete at Different Elevated Temperatures under Different Sealing Conditions

The shrinkage behavior of high performance cement concrete made from Portland cement, ultra fine granulated blast furnace slag and pulverized fly ash with addition of superplasticizer at different temperatures from ambient temperature to 120 ℃ under different seuliug conditions was investigated by means of length change measurement on cylindrical concrete specimens along with curing age. Results show that drying shrinkage deformations of titled concrete specimens increased rapidly as the curing temperature rose. The development of dryiing shrinkage deformatian can be efficiently controlled with the aid of aluminum tape sealing as compared with the unsealed specimens, especially when the curing temperature is below 60℃ , although it will increase dramatically when the curing temperature is elevated to above 90%＂ . Polymer coating on concrete specimens showed a similar effect on the control of drying shrinkage as the sealing operation with aluminum tape.

Solidification/Stabilization of Zinc-lead Tailings by Alkali Activated Slag Cement

An appropriate proportion of alkali activated slag cement, abbreviated as AASC later, was determined based on strength test of paste specimens. Results showed that AASC prepared from 14% low modulus water glass and blast furnace slag presented its compressive strength of hardened cement paste of 69.6, 84.0 and 91.8 MPa at 3, 7, and 28 d curing ages respectively. Flowability of the fresh railings-cement pastes and the strength development of hardened tailings-cement paste were also tested both in the cases with addition of AASC and Portland cement. The fresh tailings-cemant paste added with AASC presented much better flowability and the corresponding hardened paste presented higher compressive strength, especially the long term strength, than those added with Portland cement. Therefore, tallings paste added with AASC allowed lager solid content than that of Portland cement in order to keep the similar flowability. SEM observation on the microstructure of the hardened tailings-AASC mixture pastes showed obvious cementation effect. MIP measurements also showed that the total porosity of the hardened tailings-cement pastes decreased, and the portion of larger pore also decreased when the dosage of AASC increased. It is believed that AASC is more suitable to be used as a binder for the stabilization of zinc-lead railings and for its backfilling operation than Portland cement.

Cavitation-erosion mechanism of laser cladded SiC particle reinforced metal matrix composite

With 2 kW continuous wave Nd-YAG laser, SiC ceramic powder was laser-cladded on the AA6061 aluminium alloy surface. Within the range of process parameters investigated, the parameters were optimized to produce the SiC_p reinforced metal matrix composites(MMC) modified layer on AA6061 alloy surface. After being treated, the modified layer is crack-free, porosity-free, and has good metallurgical bond with the substrate. The microstructure and chemical composition of the modified layer were analyzed by such detection devices as scanning electronic microscope(SEM-EDX) and X-ray diffractometer(XRD). The performance of electrochemical corrosion and cavitation erosion and their mechanism were estimated by the microhardness tester, potentiostat and (ultrasonic-)(induced) cavitation device.

Effect of Zirconium Content on Microstructure and Magnetic Properties of Nanocomposite Bonded Magnets

Five kinds of bonded magnets with compositions of Nd(10.5)Fe(78.4-x)Co(5)Zr(x)B(6.1) (atom percentage x = 0, 1.0, 1.5, 2.0, 2.5) were prepared by rapid quenching, post heat treatment and mould-pressing. The microstructure and crystallization behavior were studied by X-ray diffraction (XRD), differential thermal analysis (DTA) and atomic force microscopy (AFM). The results suggest that high content of Zr can increase the glass formation ability (GFA) of alloys. When the content of Zr is controlled at a certain level, Fe,Zr with high melting point is formed in the alloys, and grain size is reduced consequently. At the same time, because of Zr addition, the coercivity and squareness of demagnetization loop are obviously improved, and the energy product is accordingly increased. As a result, optimal magnetic properties of Nd(10.5)Fe(78.4-x)Co(5)Zr(x)B(6.1) (B(t) = 0. 659 T, H(cj) = 628 kA center dot m(-1), H(cb) = 419 kA center dot m(-1) (BH)(m) 73 kJ center dot m(-3)) are obtained when x = 2.

Thermal, Mechanical and Electrical Properties of the PEO-based Solid Polymer Electrolytes Filled by Yttrium Oxide Nanoparticles

The novel composite lithium solid polymer electrolytes （SPEs） composed of polyethylene oxide （PEO） matrix and yttrium oxide （Y2O3） nanofillers were prepared by a solution casting method. The crystal morphology of the SPEs was characterized by polarized optical microscope （POM） and wide-angle X-ray diffraction （WAXD）. The induced nucleation and steric hindrance effects of Y2O3 nanofillers result in the increased amount as well as decreased size of PEO spherulites which are closely related to the crystallinity of the SPEs. As the Y2O3 contents increase from 0 wt% to 15 wt%, the crystallinity of the SPEs decreases proportionally. The thermal, mechanical and electrical properties of the SPEs were investigated by thermal gravimetric analysis （TGA）, dynamic mechanical analysis （DMA） and AC impedance method, respectively. The physical properties including thermal, mechanical and electrical performances, depending remarkably on the polymer-filler interactions between PEO and Y2O3 nanoparticles, are improved by different degrees with the increase of Y2O3 contents. The （PEO）21LiI/10 wt%Y2O3 composite SPE exhibits the optimal room-temperature ionic conductivity of 5.95×10-5 Scm-1, which satisfies the requirements of the conventional electrochromic devices.

Activating Process of Geopolymer Source Material: Kaolinite

The calcining process was recorded by differential scanning calorimetry and ther-mogravimetry （DSC-TG）. The dehydroxylation （activating process） was partitioned into two steps by calculating and comparing the O-H bond lengths between inner hydroxyl group and surface hydroxyl group, as well as the ionic bond of Al-OH and position of -OH. X-ray diffraction （XRD） and compressive strength measurement show that the activity of calcined materials increases with the increasing of temperature in dehydroxylation region but decreases abruptly in the ＂spinel＂ region. The suggested temperature for activating kaolinite is 900 ℃ .

Synthesis, Structure and Luminescent Property of a New Zn(Ⅱ) Coordination Polymer Based on 1,3,5-Benzenetricarboxylate and 4,4'-Bipyridine Ligands

A new Zn（II） coordination polymer [Zn3（BTC）2（4,4＇-bpy）（CO）2]n （1, H3BTC = 1,3,5-benzenetricarboxylic acid, 4,4＇-bpy = 4,4＇-bipyridine） has been prepared through urothermal reaction of zinc nitrate hexahydrate with 1,3,5-benzenetricarboxylic acid and 4,4＇-bipyridine, and characterized by elemental analysis, IR spectroscopy, TGA and powder XRD, and its crystal structure was determined by single-crystal X-ray diffraction analysis. The title compound crystallizes in the monoclinic system, space group C2/c, with a = 10.262（3）, b = 18.838（5）, c = 15.083（4）/k, fl = 99.203（4）°, V = 2878.3（14） A3, C30H14Zn3N2O14, Mr= 822.54, Z = 4, Dc = 1.898 g/cm3,μ = 2.561 mm-1,F（000） = 1640, R = 0.0363 and wR = 0.0932 for 2828 observed reflections （I 〉 2σ（I））. X-ray analysis shows that the asymmetric unit of the title compound contains two crystallographically unique Zn（lI） atoms which are connected by BTC3- ligands and 4,4＇-bpy coligands to form a 3D framework with 1D channels. The solid luminescence of ligand and the title complex was also studied at room temperature.

Crystallization Behavior of Copolymer Poly(ethylene terephth-alate/isophthalate)(IPET)

The non-isothermal crystallization kinetics, isothermal crystallization and the morphology of crystals of the copolymer poly (ethylene terephthalate/ isophthalate )(IPET) were studied by DSC and polarized-light microscopy in this paper. DSC results indicate that the glass transition temperature Tg of IPET is slightly lower than that of poly(ethylene terephthalate) (PET), but the melting temperature Tm and the crystallization temperature Tc of PET and IPET have much difference.The difference of Tc between PET and IPET2 is about 7℃, and the difference of Tm between PET and IPET2 is about 16℃. From the kinetics analysis of the crystallization, the crystallization mechanism of all samples is of three-dimension spherulitic growth from instantaneous nuclei and the incorporation of isophthalate (IPA) decreases the crystallization rate of IPET greatly. The isothermal results indicate that the morphologies of PET and IPET crystals are all spherulite, which is in conformity to the results of nonisothermal dynamic crystallization. At the same time,the spherulite of IPET grows slower and has longer incubation time than the spherulite of PET under the same crystallization condition.

Electrical resistance stability of high content carbon fiber reinforced cement composite

The influences of curing time, the content of free evaporable water in cement paste, environmental temperature, and alternative heating and cooling on the electrical resistance of high content carbon fiber reinforced cement (CFRC) paste are studied by experiments with specimens of Portland cement 42.5 with 10 mm PAN-based carbon fiber and methylcellulose. Experimental results indicate that the electrical resistance of CFRC increases relatively by 24% within a hydration time of 90 d and almost keeps constant after 14 d, changes hardly with the mass loss of free evaporable water in the concrete dried at 50 °C, increases relatively by 4% when ambient temperature decreases from 15 °C to ?20 °C, and decreases relatively by 13% with temperature increasing by 88 °C. It is suggested that the electric resistance of the CFRC is stable, which is testified by the stable power output obtained by electrifying the CFRC slab with a given voltage. This implies that such kind of high content carbon fiber reinforced cement composite is potentially a desirable electrothermal material for airfield runways and road surfaces deicing.

Microstructure and corrosion mechanism of as-cast Mg-Zn-Mn-Ca in Hank's solution

An Mg-Zn-Mn-Ca alloy with high Zn content was fabricated by vacuum melting.The as-cast microstructure was investigated using XRD,SEM and EDS.It was shown that the alloy was composed of α-Mg,strip-like Ca2Mg6Zn3 and a few Mncontaining phases.Most of the Ca2Mg6Zn3 phase was distributed at grain boundaries while Mn-containing particles were deposited within grains.The as-cast samples were immersed in a Hank's balanced salt solution(HBSS) up to 24 h.The corroded surface morphology and cross-section microstructure were analyzed after different time of immersion so as to understand the corrosion behavior of the alloy.During immersion in the HBSS,the alloy corroded homogeneously at the very beginning and then localized corrosion occurred.The secondary phases protruded on the surface due to the dissolution of α-Mg,suggesting microgalvanic corrosion occurred with secondary phases acting as the cathode and α-Mg as the anode.Micro-cracks were formed at the interfaces between Ca2Mg6Zn3 and α-Mg,indicating an undermining tendency of the secondary phases.