Fe-Ni-Al mixtures as hot-pressing sintering additive to Titanium diboride （TiB2） were studied. It is found that liquid alloy formed under high temperature hardly has effects on the densification behaviors of TiB2-in...
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Fe-Ni-Al mixtures as hot-pressing sintering additive to Titanium diboride （TiB2） were studied. It is found that liquid alloy formed under high temperature hardly has effects on the densification behaviors of TiB2-independent. Fe-Ni-Al additive just works as filler between TiB2 particles and does not change the TiB2-independent sintering behaviors. Pressing mode has a great effect on the liquid flowing between TiB2 particles. Multiple-steps pressing mode will give more time and space for the liquid flowing and improve the relative density of TiB2-Fe-Ni-Al cermet.
Preparation and thermoelectric properties of nanostructured n-type Mg2Si bulk materials were reported. Nanosized Mg2Si powder was obtained by mechanical milling of the microsized Mg2Si powder prepared by solid-state r...
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Preparation and thermoelectric properties of nanostructured n-type Mg2Si bulk materials were reported. Nanosized Mg2Si powder was obtained by mechanical milling of the microsized Mg2Si powder prepared by solid-state reaction. The bulk materials with 30 nm and 5 μm were prepared by spark plasma sintering of the nanosized and microsized Mg2Si powder, respectively. Both the samples show n-type conduction and the Seebeck coefficient of the sintered samples increase determinately with the grain size decrease from 5 μm to 30 nm. On the other hand, the electrical and thermal conductivity decrease with the decrease of grain size. Accordingly, decreasing their grain size increases their thermoelectric-figure-of-merit. A maximum thermoelectric figure of merit of 0.36 has been obtained for the nanostuctured Mg2Si sample at 823 K, which is 38% higher than that of microsized Mg2Si bulk materials and higher than results of other literatures. It could be expected that the properties of the nanocomposites could be further improved by doping optimization.
Flame retardant epoxy resins were prepared by a simple mixed method using ammonium aluminum carbonate hydroxy hydrate （AACHH） as a halogen-free flame retardant. The prepared samples were characterized by X-ray diffr...
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Flame retardant epoxy resins were prepared by a simple mixed method using ammonium aluminum carbonate hydroxy hydrate （AACHH） as a halogen-free flame retardant. The prepared samples were characterized by X-ray diffraction, thermogravimetric and differential scanning calorimetry, scanning electron microscope and limiting oxygen index（LOI） experiments. Effects of AACHH content on LOI of epoxy resins/AACHH composite and flame retardant mechanism were investigated and discussed. Results show that AACHH exhibites excellent flame-retardant properties in epoxy resin（EP）. When the content of AACHH was 47.4%, the LOI of EP reached 32.2%. Moreover, the initial and terminal decomposition temperature of EP increased by 48 ℃ and 40 ℃, respectively. The flame retarded mechanism of AACHH is due to the synergic flame retardant effects of diluting, cooling, decomposition resisting and obstructing.
Low or zero thermal expansion porous ceramics are required for several applications. In this work near zero thermal expansion porous ceramics were fabricated by using SiC and ZrW2O8 as positive and negative thermal ex...
Low or zero thermal expansion porous ceramics are required for several applications. In this work near zero thermal expansion porous ceramics were fabricated by using SiC and ZrW2O8 as positive and negative thermal expansion materials, respectively, bonded by soda lime glass. The mixture of SiC, ZrW2O8 and soda lime glass was sintered by Pulsed Electric Current Sintering (PECS, or sometimes called Spark Plasma Sintering, SPS) at 700 °C. Sintered samples with ZrW2O8 particle size smaller than 25 μm have high thermal expansion coefficient, because ZrW2O8 has the reaction with soda lime glass to form Na2ZrW3O12 during sintering process. The reaction between soda lime glass and ZrW2O8 is reduced by increasing particle size of ZrW2O8. Sintered sample with ZrW2O8 particle size 45-90 μm shows near zero thermal expansion.
N-type Si-based type-Ⅰ clathrates with different Ga content were synthesized by combining the solid-state reaction method,melting method and spark plasma sintering （SPS） *** effects of Ga composition on high temper...
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N-type Si-based type-Ⅰ clathrates with different Ga content were synthesized by combining the solid-state reaction method,melting method and spark plasma sintering （SPS） *** effects of Ga composition on high temperature thermoelectric transport properties were *** results show that at room temperature,the carrier concentration decreases, while the carrier mobility increases slightly with increasing Ga *** Seebeck coefficient increases with increasing Ga content. Among all the samples,Ba7.93Ga17.13Si28.72exhibits higher Seebeck coefficient than the others and reaches -135μV·K^-1 at 1000 *** sample prepared by this method exhibits very high electrical conductivity,and reaches 1.95x 10^5 S·m^-1 for Ba8.01Ga16.61Si28.93 at room *** thermal conductivity of all samples is almost temperature independent in the temperature range of 300-1000 K,indicating the behaviour of a typical *** maximum ZT value of 0.75 is obtained at 1000 K for the compound Ba7.93Ga17.13Si28.72.
A solution method was developed for fabricating ZnO nanostructures using （NH4）2CO3 as starting material SEM analysis shows that ZnO nanostructures exhibit nanorod, branch and flower-like morphologies. The crystal ph...
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A solution method was developed for fabricating ZnO nanostructures using （NH4）2CO3 as starting material SEM analysis shows that ZnO nanostructures exhibit nanorod, branch and flower-like morphologies. The crystal phase of as-synthesized products was characterized by X-ray diffraction （XRD）. The growth process, formation mechanism and optical property were also discussed by means of transmission electronic microscopy （TEM）, high resolution transmission microscopy （HRTEM） and photoluminescence （PL）. The growth direction of ZnO nanostructures was investigated based on the results of HRTEM. The PL spectrum shows two strong peaks （centered at around -387 and -470 nm） and a broad Deak （centered at around -580 nm）.
A series of new polyamides 3a-d containing aryl-azo, ether and sulfone groups in the main chain were synthesized from bis[4-（4-aminophenoxy）phenyl sulfone] 1 and several azo aromatic diacyl chlorides 2a-d by the low...
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A series of new polyamides 3a-d containing aryl-azo, ether and sulfone groups in the main chain were synthesized from bis[4-（4-aminophenoxy）phenyl sulfone] 1 and several azo aromatic diacyl chlorides 2a-d by the low temperature solution polycondensation technique. FTIR spectroscopy, nuclear magnetic resonance （NMR） and elemental analyses confirmed the structure of these polymers. Owing to the aryl and amide groups in the main chain, these polymers exhibit photochromic properties as well as excellent thermal stabilities. The transition temperatures （Tg） are between 242 and 265℃, and the char yields at 800 ℃ in nitrogen atmosphere were above 39%. Based on incorporation of flexible ether linkages and polar sulfone groups, the polyamides show desirable solubility in organic solvents such as DMAc, N,N-dimethylformamide （DMF）, N-methyl-2-pyrroidinone （NMP） and dimethylsulfoxide （DMSO）. And it is exemplified that polyamide containing 2 and 2＇ substitutes performed better solubility.
Flame-retardant mechanism of magnesium oxychloride （M OC） in EP was in-vestigated by limiting oxygen index （LOI）, XRD, SEM, TG-DTG and DSC. The results show that MOC performed well as an inorganic flame-retardant ...
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Flame-retardant mechanism of magnesium oxychloride （M OC） in EP was in-vestigated by limiting oxygen index （LOI）, XRD, SEM, TG-DTG and DSC. The results show that MOC performed well as an inorganic flame-retardant in EP. When the content of MOC is 50%, the LOI of EP reaches 29.6% and mass of residual char reaches 9.6%. The flame retarde mechanism of MOC is due to the synergies of diluting, cooling, catalyzing char forming and obstructing effects.
Silver powder was fabricated by spray pyrolysis, using 2%-20% AgNO3 solution, 336-500 mL/h flux of AgNO3 solution, 0.28-0.32 MPa flux of carrier gas and in the 620-820 ℃ temperature range. The effects of furnace set ...
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Silver powder was fabricated by spray pyrolysis, using 2%-20% AgNO3 solution, 336-500 mL/h flux of AgNO3 solution, 0.28-0.32 MPa flux of carrier gas and in the 620-820 ℃ temperature range. The effects of furnace set temperature, concentration of AgNO3 aqueous solution, flux of AgNO3 aqueous solution as well as carrier gas on the morphology and particle size distribution of silver powder, were investigated. The experimental results showed that with the high concentration of AgNO3 aqueous solution, the average grain size of silver decreased with the increasing of furnace set temperature. But the gain size distribution was not homogenous, the discontinuous grain growth occurred. With the low concentration of AgNO3 aqueous solution, the higher furnace set temperature made the nano sliver grains sintered together to grow. Nano silver powder about 100 nm was fabricated by spray pyrolysis, using 2wt% AgNO3 solutions, 336 mL/h flux of AgNO3 aqueous solution, 0.32 MPa flux of carrier gas at 720 ℃ furnace set temperature.
The spherical agglomerated particles were fabricated by spray drying with the powders of NiO, Cr2O3 and TiO2. Plasma spray power, which has good property of flowability, was acquired by heat treatment from the particl...
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The spherical agglomerated particles were fabricated by spray drying with the powders of NiO, Cr2O3 and TiO2. Plasma spray power, which has good property of flowability, was acquired by heat treatment from the particles at 1200℃ in the reducing atmosphere. Dark and uniform coating of More than 50 μm thick was deposited on the copper sheet substrate by plasma spraying. It is found that the infrared normal total emissivity of the coating is up to 0.91 at 600℃ by infrared radiation testing. The X-ray diffraction analysis shows that the formation of （Cr0.88Ti0.12）2O3 and spinel structural NiCr2O4 in the coating is the main reason for high efficient infrared radiation, and the phase structure and performance of coating is favorable under the thermal cycle between room temperature and 600℃.
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