Fabrication of Y_2Si_2O_7 coating and its oxidation protection for C/SiC composites

Yttrium silicate （Y2Si2O7） coating was fabricated on C/SiC composites through dip-coating with silicone resin ＋ Y2O3 powder slurry as raw materials. The synthesis, microstructure and oxidation resistance and the anti-oxidation mechanism of Y2Si2O7 coating were investigated. Y2Si2O7 can be synthesized by the pyrolysis of Y2O3 powder filled silicone resin at mass ratio of 54.2：45.8 and 800 °C in air and then heat treated at 1400 °C under Ar. The as-fabricated coating shows high density and favorable bonding to C/SiC composites. After oxidation in air at 1400, 1500 and 1600 °C for 30 min, the coating-containing composites possess 130%-140% of original flexural strength. The desirable thermal stability and the further densification of coating during oxidation are responsible for the excellent oxidation resistance. In addition, the formation of eutectic Y-Si-Al-O glassy phase between Y2Si2O7 and Al2O3 sample bracket at 1500 °C is discovered.

矿物掺合料对C100～C120超高强混凝土基本性能的影响

通过正交试验考察了胶凝材料总量、水泥用量及超细粉煤灰用量对超高强混凝土抗压强度的影响,研究了硅灰、超细粉煤灰与复合硅材等矿物掺合料对C100~C120超高强混凝土基本性能的影响。结果表明,对超高强混凝土强度影响最主要的因素是水泥在胶凝材料中所占的比例;超细粉煤灰与硅灰复掺对超高强混凝土工作性能与强度改善效果较好;复合硅材对超高强混凝土的工作性能与强度均有一定的提高。

Preparation of three-dimensional interconnected mesoporous anatase TiO_2-SiO_2 nanocomposites with high photocatalytic activities

In this article, we report the preparation of a three-dimensional（3D） interconnected mesoporous anatase TiO2-SiO2 nanocomposite. The nanocomposite was obtained by using an ordered two-dimensional（2D） hexagonal mesoporous anatase 70 TiO2-30 SiO2-950 nanocomposite（crystallized at 950 °C for 2 h） as a precursor, NaO H as an etchant of SiO2 via a ＂creating mesopores in the pore walls＂ approach. Our strategy adopts mild conditions of creating pores such as diluted NaO H solution, appropriate temperature and solid/liquid ratio, etc. aiming at ensuring the integrities of mesopores architecture and anatase nanocrystals. XRD, TEM and N2 sorption techniques have been used to systematically investigate the physico-chemical properties of the nanocomposites. The results show that the intrawall mesopores are highly dense and uniform（average pore size 3.6 nm）, and highly link the initial mesochannels in a 3D manner while retaining mesostructural integrity. There is no significant change to either crystallinity or size of the anatase nanocrystals before and after creating the intrawall mesopores. The photocatalytic degradation rates of rhodamine B（RhB, 0.303 min^–1） and methylene blue（MB, 0.757 min^–1） dyes on the resultant nanocomposite are very high, which are 5.1 and 5.3 times that of the precursor; even up to 16.5 and 24.1 times that of Degussa P25 photocatalyst, respectively. These results clearly demonstrate that the 3D interconnected mesopores structure plays an overwhelming role to the increments of activities. The 3D mesoporous anatase TiO2-SiO2 nanocomposite exhibits unexpected-high degradation activities to RhB and MB in the mesoporous metal oxide-based materials reported so far. Additionally, the nanocomposite is considerably stable and reusable. We believe that this method would pave the way for the preparation of other 3D highly interconnected mesoporous metal oxide-based materials with ultra-high performance.

EFFECT OF COMPOSITE MINERAL ADMIXTURES ON RESTRAINING ALKALI-SILICA REACTION

The expansion and micro-cracks of the mortar with composite mineral admixtures （fly ash, zeolite and slag） due to the alkali-silica reaction （ASR） are studied. Results show that composite mineral admixtures cannot absolutely diminish the ASR of mortar bars with the low-alkali cement and a highly reactive aggregate. But the expansion rate and the deleterious expansion of the mortar bar are mostly reduced with increasing composite mineral admixture. The influence of mineral admixtures on the fluidity of the paste and the strength of the mortar is also studied.

The Effect of Silane Grafted Polypropylente on the Property of Different Filler/Polypropylene Composites

Aim To determine the effect of silane grafted polypropylene on the property of different filler/polypropylene composites. Methods Polypropylene (PP) composites filled with talc(Ta), baryta sulfate and calcium carbonate coupled with silane grafted polypropylene (PP-g-Si) were made, their mechanical properties and thermal properties were investigated, respectively. Results As compared with the non-coupled composites, the mechanical properties of PP/Ta/PP-g-Si composites were improved to some extent, though the values of tensile modulus and the strain at peak were decreased. But for PP/BaSO4 and PP/CaCO3 composites, the values of their mechanical properties varied slightly or even decreased with increasing PP-g-Si content within the experimental component. Meanwhile, PP-g-Si also affected the melting and crystallization behavior of PP in the composites. Conclusion PP-g-Si offers compatibilization in PP/Ta composites, but offers no-compatibilization in PP/BaSO4 and PP/CaCO3 composites within the extent of the present range of PP-g-Si, which shows that PP-g-Si can be used as the macromolecular coupling agent of PP and Ta composite.

PIEZOSPECTROSCOPIC STUDY OF RESIDUAL STRESSES AROUND INDENTATIONS IN SiC/Al_O_3 NANOCOMPOSITE

A new experimental measurement of residual stresses around Vickers′ indentations on the surface of the SiC/Al 2O 3 nanocomposites is proposed with the aid of a Raman microprobe. Results s how that the shifts of R lines in the fluorescence spectra va ry with the distance from the centre of indentation. The magnitude of load appli ed on the surface of the materials through the indenter influences the shifts of R lines to great extent. The luminescence of R lines of the materials before indenting is used to determine the residual stresses around the indentation in the materials, assuming that the stress tensor is transversely isotropic. Final ly, the term of hydrostatic stress is adopted to explain and compare different residual stresses around indentations with the increase of the indenting load an d the distance from the centre of indentations. <

Fabrication,characterization and electrochemical properties of porous coral-structured Si/C composite anode for lithium ion battery

A porous coral-structured Si/C composite as an anode material was fabricated by coating Si nanoparticles with a carbon layer from polyvinyl alcohol（PVA）, erosion of hydrofluoric（HF） acid, and secondary coating with pitch. Three samples with different pitch contents of 30%, 40% and 50% were synthesized. The composition and morphology of the composites were characterized by X-ray diffractometry（XRD） and scanning electron microscopy（SEM）, respectively, and the properties were tested by electrochemical measurements. The results indicated that the composites showed obviously enhanced electrochemical performance compared with that without secondary carbon coating. The second discharge capacity of the composite was 773 m A·h/g at a current density of 100 m A/g, and still retained 669 m A·h/g after 60 cycles with a small capacity fade of less than 0.23%/cycle, while the content of secondary carbon source of pitch was set at 40%. Therefore, the cycle stability of the composite could be excellently improved by regulating carbon content of secondary coating.

Study on mechanical properties of composite materials by in-situ tensile test

The mechanical properties of the SiC fiber-reinforced Mg-Al metal matrix composite materials have been studied on internal microstructure by (scanning electron microscopy) SEM in-situ tensile test. The emergence and propagation of the crack, and the fracture behavior in materials have been observed and studied. It is found that in the case of the tensile test, the crack emerged in SiC fiber initially. In the case of the strong cohesion of the fiber-metal interface, the crack propagated in the fiber, meanwhile the fibers in the neighborhood of the cracked fiber began to crack and the Mg-Al metal deformed plastically, and at last the material fractured. Otherwise the toughness of the materials grows in the case of the lower cohesion of the fiber-metal matrix interface.

Preparation and Flame Retardancy of Polyurethane/POSS Nanocomposites

Polyurethane/polyhedral oligomeric sisesquioxane （PU/POSS） nanocomposites were syn- thesized via polymerization utilizing the compatibility between POSS nanopartieles and 4J-diphenyl methylene diisocyanate. Scanning electron microscope images and Fourier transform infrared spectra revealed that POSS nanoparticles were dispersed in PU matrix. Thermal gravimetric analysis was employed to investigate the thermal decomposition be- havior of PU/POSS nanocomposites at elevated temperatures. Then fire performance was evaluated by limiting oxygen index, underwriters laboratories 94 testing and char residue morphology. These results showed that the addition of POSS promoted the formation of char residues which were covered on the surface of polymer composites, leading to the ira-provement of thermal stability and flame retardancy.

Tribological behavior of friction stir processed SiP/ZA40 in-situ composites

The effect of friction stir processing(FSP)at different rotation speeds(400,630,800,and 1000 r/min)and traverse speeds(25 and 50 mm/min)on the tribological properties of a Si particle reinforced Zn−40Al−2Cu-based in-situ composite was investigated.After preliminary optimization,800 r/min and 25 mm/min were selected as optimum FSP parameters.According to the results,multi-pass FSP improved the tribological properties.For instance,at an applied pressure of 0.75 MPa,the wear rate and average coefficient of friction(COF)of four-pass FSPed composite were lower than those of base composite by 53%and 50%,respectively.SEM examinations of worn surfaces,wear debris,and worn subsurfaces revealed that the intensive refinement and uniform distribution of microstructural phases,especially the coarse Si particles,reduced Si particles interspacing,and elimination of casting defects were the most important factors enhancing the substrate resistance against sliding-induced deformation.This led to the formation of stable tribolayers that improved the tribological properties.

Surface Modification of Nanometer TiO_2 and Effect of Preparing TiO_2/P(St-co-DVB) Composites by Dispersion Polymerization

Surface modification of nanometer titanium dioxide particles and effect of preparing TiO2/P （St-co-DVB） composites by dispersion polymerization are described. To introduce vinyl group onto the surface of titanium dioxide particles, the titanium dioxide particles were surface-modified with a silicane coupling agent, methacryloylpropyltrimethoxysilicane. Polymer encapsulation in the presence of either modified-titanium dioxide particles or unmodified-titanium dioxide particles was carried out by dispersion polymerization of styrene, divinylbenzene in ethanol medium with polyvinylpyrroliclone as stabilizer, and 2, 2＇-azobis（isobutyronitrile） as initiator. The modified-titanium dioxide was analyzed with Fourier-transform infrared spectroscopy（FTIR）, UV-Vis spectrophotometer, thermo-gravimetric analysis and transmission microscope. The polymer encapsulation of modified-titanium dioxide and unmodified-titanium dioxide particles was confirmed with FTIR and transmission electron microscope. Results show that compared with unmodified-titanium dioxide, modified-titanium dioxide is more suitable for preparing inorganic core/orclanic shell composites.

Effect of SiC content on dry sliding wear, corrosion and corrosive wear of Al/SiC nanocomposites

The corrosion, corrosive wear and dry sliding wear of nanocomposites, are extremely complicated and involve various chemical, physical anbd mechanical factors. The aim of this work is to investigate the effects of nanosized SiC content on the hardness, dry sliding wear, corrosion and corrosive wear of Al/SiC nanocomposites synthesized by mechanical milling cold pressing and hot extrusion. The corrosion resistance of these composites in 3%NaCl solution was investigated by electrochemical polarization testing and their dry sliding as well as corrosive wear resistance in the same solution was evaluated using a pin-on-disc tester. The microstructures of the samples and their worn surfaces were examined using scanning electron microscopy. It was shown that the dry sliding wear and corrosion resistance of these nanocomposites were improved with the increase of SiC content. It was concluded that due to the lubrication effect of the solution, both the friction coefficient and frictional heat that might soften the material were reduced. In addition, the improved strength of the nanocomposites combined with their better corrosion resistance contributed to their increased corrosive wear resistance, compared with the base alloy. The prominent wear mechanism in the unreinforced alloy was adhesive wear, in the Al/SiC nanocomposites, the wear mechanism changed to abrasive.

Ductility and hardness of chloride cleaned AA6011/SiC_p composites

Theductility and hardness of AA6011/SiCp composites using NaCl, SnCl2, NH4Cl and PdCl2 as wetting reagents were investigated. SiCp was cleaned with the wetting reagents, and used as reinforcement in AA6011 alloy using the stir casting method. Ductility and hardness responses of the composites were measured using standard methods. Microstructural features were examined using scanning electron microscopy and the phases were determined with the help of an X-ray diffractometer. The results show that for all wetting agents, the increase in cleaning time leads to initial increase in ductility to a certain value, but a decrease afterwards with further increase in cleaning time. The best combination of hardness （BHN 57.88） and ductility （11.91%） was shown under conditions of 40 g/L SnCl2and cleaning time of 60 min. A minor formation of Al4C3was noted in diffraction patterns, indicating that the formation of deleterious precipitate was hindered by the cleaning process.

Preparation of Composite Microporous Silica Membranes Using TEOS and 1,2-Bis(triethoxysilyl)ethane as Precursors for Gas Separation

This paper reports on a new microporous composite silica membrane prepared via acid-catalyzed polymeric route of sol-gel method with tetraethylorthosilicate(TEOS)and a bridged silsesquioxane[1,2-bis(triethoxysilyl)ethane, BTESE]as precursors.A stable nano-sized composite silica sol with a mean volume size of^5 nm was synthesized. A 150 nm-thick defect-free composite silica membrane was deposited on disk support consisting of macroporous α-Al2O3 and mesoporousγ-Al2O3 intermediate layer by using dip-coating approach,followed by calcination under pure nitrogen atmosphere.The composite silica membranes exhibit molecular sieve properties for small gases like H2,CO2,O2,N2,CH4 and SF6 with hydrogen permeances in the range of(1-4)×10 -7mol·m -2·s -1·Pa -1(measured at 200°C,3.0×105 Pa).With respect to the membrane calcined at 500°C,it is found that the permselectivities of H 2 (0.289 nm)with respect to N2(0.365 nm),CH4(0.384 nm)and SF6(0.55 nm)are 22.9,42 and>1000,respectively, which are all much higher than the corresponding Knudsen values(H2/N2=3.7,H2/CH4=2.8,and H2/SF6=8.5).

Wet friction performance of C/C-SiC composites prepared by new processing route

C/C-SiC composites with SiC island distribution Were prepared via a new processing route. The fabrication process mainly included silicon infiltration by ultrasonic vibration, chemical vapor deposition （CVD）, siliconizing, liquid phase impregnation and carbonization. The wear and friction properties were tested by an MM-1000 wet friction machine. The results show that SiC phases are mainly distributed between carbon fibers and pyrocarbons as well as among the pryoearbons. The dynamic friction coefficient of the composites decreases gradually from 0.126 to 0.088 with the increase of the surface pressure from 0.5 to 2.5 MPa at the same rotary speed. Furthermore, under the constant surface pressure, the dynamic friction coefficient increases from 0.114 to 0.126 with the increase of the rotary speed from 1 500 to 2 500 r/min. However, the coefficient decreases to 0.104 when the rotary speed exceeds 4 500 r/min. During the friction process, the friction coefficient of C/C-SiC composite is between 0.088 and 0.126, and the wear value is zero after 300 times brake testing.

Microstructure and properties of alumina-silicon carbide nanocomposites fabricated by pressureless sintering and post hot-isostatic pressing

A1203/5%SIC nanocomposites were fabricated by pressureless sintering using MgO as a sintering aid and then post hot-isostatic pressed （HIP）, which can subsequently break through the disadvantage of hot-pressing process. The MgO additive was able to promote the densification of the composites, but could not induce the grain growth of A1203 matrix due to the grain growth inhibition by nano-sized SiC particles. After HIP treatment, A12OJSiC nanocomposites achieved full densification and homogeneous distribution of nano-sized SiC particles. Moreover, the fracture morphology of HIP treated specimens was identical with that of the hot-pressed A1203/SiC nanocomposites showing complete transgranular fracture. Consequently, high fracture strength of 1 GPa was achieved for the A1203/5%SIC nanocomposites by pressureless sintering and post HIP process.

Effects of SiC amount on phase compositions and properties of Ti_3SiC_2-based composites

The phase compositions and properties of Ti3SiC2-based composites with SiC addition of 5%-30% in mass fraction fabricated by in-situ reaction and hot pressing sintering were studied. SiC addition effectively prevented TiC synthesis but facilitated SiC synthesis. The Ti3SiC2/Ti C-SiC composite had better oxidation resistance when SiC added quantity reached 20% but poorer oxidation resistance with SiC addition under 15% than Ti3SiC2/TiC composite at higher temperatures. There were more than half of the original SiC and a few Ti3SiC2 remaining in Ti3SiC2/Ti C-SiC with 20% SiC addition, but all constituents in Ti3Si2/TiC composite were oxidized after 12 h in air at 1500 °C. The oxidation scale thickness of TS30, 1505.78 μm, was near a half of that of T,2715 μm, at 1500 °C for 20 h. Ti3SiC2/Ti C composite had a flexural strength of 474 MPa, which was surpassed by Ti3SiC2/TiC-SiC composites when SiC added amount reached 15%. The strength reached the peak of 518 MPa at 20% SiC added amount.

Preparation and Characterization of Sodium Sulfate/Silica Composite as a Shape-stabilized Phase Change Material by Sol-gel Method

A sodium sulfate （NaeSO4）/silica （SiO2） composite was prepared as a shape-stabilized solid-liquid phase change material by a sol-gel procedure using Na2SiO3 as the silica source. Na2SO4 in the composite acts as a latent heat storage substance for solid-liquid phase change, while SiO2 acts as a support material to provide structural strength and prevent leakage of melted NazSO4. The microstructure and composition of the prepared composite were characterized by the N2 adsorption, transmission electron microscope （TEM）, scanning electron microscope （SEM）, Fourier transform infrared spectroscopy （FTIR） and X-ray diffraction. The results show that the prepared Na2SOJSiO2 composite is a nanostructured hybrid of NazSO4 and SiO2 without new substances produced during the phase change. The macroscopic shape of the NazSO4/SiO2 composite after the melting and freezing cycles does not change and there is no leakage of Na2SO4. Determined by differential scanning calorimeter （DSC） analysis, the values of phase change latent heat of melting and freezing of the prepared NazSO4/SiO2 （50%, by mass） composite are 82.3 kJ.kg i and 83.7 kJ.kg-1, and temperatures of melting and freezing are 886.0 ℃ and 880.6 ℃, respectively. Furthermore, the Na2SOJSiO2 composite maintains good thermal energy storage and release ability even after 100 cycles of melting and freezing. The satisfactory thermal storage performance renders this composite a versatile tool for high-temperature thermal energy storage.

Effect of laser surface melting on surface integrity of Al-4.5Cu composites reinforced with SiC and MoS2

Two types of composites were prepared with Al-4.5Cu alloy as a matrix using stir casting method.One was reinforced with 10wt.%of Si C and 2wt.%of MoS2.The other was reinforced with 10wt.%of Si C and 4wt.%of MoS2.Their surfaces were remelted using a CO2 laser beam with an objective to study the influence of laser surface melting(LSM).The topography,microhardness,corrosion resistance and wear resistance of the laser melted surfaces were studied.Overall surface integrity after LSM was compared with as-cast surface.LSM enhanced the microhardness and wear resistance of the surface in each case.Porosity of the laser melted surface was low and corrosion resistance was high.Thus,LSM can be conveniently applied to enhancing the surface integrity of the aluminium composites.However,there is an optimum laser specific energy,around 38 J/m^2 in this study,for obtaining the best surface integrity.

Dynamic recrystallization and silicide precipitation behavior of titanium matrix composites under different strains

In order to elucidate the microstructure evolution and silicide precipitation behavior during high-temperature deformation,TiB reinforced titanium matrix composites were subjected to isothermal hot compression at 950℃,strain rate of 0.05 s^(−1) and employing different strains of 0.04,0.40,0.70 and 1.00.The results show that with the increase of strain,a decrease in the content,dynamic recrystallization of theαphase and the vertical distribution of TiB along the compression axis lead to stress stability.Meantime,continuous dynamic recrystallization reduces the orientation difference of the primaryαphase,which weakens the texture strength of the matrix.The recrystallization mechanisms are strain-induced grain boundary migration and particle stimulated nucleation by TiB.The silicide of Ti_(6)Si_(3) is mainly distributed at the interface of TiB andαphase.The precipitation of silicide is affected by element diffusion,and TiB whisker accelerates the precipitation behavior of silicide by hindering the movement of dislocations and providing nucleation particles.