Gypsum was used as substrate,and silica gel was mixed into substrate at a certain mass ratio to prepare humidity-controlling composites;moreover,the moisture absorption and desorption properties of gypsum-based compos...Gypsum was used as substrate,and silica gel was mixed into substrate at a certain mass ratio to prepare humidity-controlling composites;moreover,the moisture absorption and desorption properties of gypsum-based composites were compared with adding different silica gel particle size and proportion.The morphological characteristics,the isothermal equilibrium moisture content curve,moisture absorption and desorption rate,moisture absorption and desorption stability,and humidity-conditioning performance were tested and analyzed.The experimental results show that,compared with pure-gypsum,the surface structure of the gypsum-based composites is relatively loose,the quantity,density and aperture of the pores in the structure increase.The absorption and desorption capacity increase along with the increase of silica gel particle size and silica gel proportion.When 3 mm silica gel particle size is added with a mass ratio of 40%,the maximum equilibrium moisture content of humidity-controlling composites is 0.161 g/g at 98% relative humidity(RH),3.22 times that of pure-gypsum.The moisture absorption and desorption rates are increased,the equilibrium moisture absorption and desorption rates are 2.68 times and 1.61 times that of pure-gypsum at 58.5% RH,respectively.The gypsum-based composites have a good stability,which has better timely response to dynamic humidity changes and can effectively regulate indoor humidity under natural conditions.展开更多
As one of the most widely used personal protective equipment(PPE),body armors play an important role in protecting the human body from the high-velocity impact of bullets or projectiles.The body torso and critical org...As one of the most widely used personal protective equipment(PPE),body armors play an important role in protecting the human body from the high-velocity impact of bullets or projectiles.The body torso and critical organs of the wear may suffer severe behind-armor blunt trauma(BABT)even though the impactor is stopped by the body armor.A type of novel composite material through incorporating shear stiffening gel(STG)into ethylene-vinyl acetate(EVA)foam is developed and used as buffer layers to reduce BABT.In this paper,the protective performance of body armors composed of fabric bulletproof layers and a buffer layer made of foam material is investigated both experimentally and numerically.The effectiveness of STG-modified EVA in damage relief is verified by ballistic tests.In parallel with the experimental study,numerical simulations are conducted by LS-DYNA®to investigate the dynamic response of each component and capture the key mechanical parameters,which are hardly obtained from field tests.To fully describe the material behavior under the transient impact,the selected constitutive models take the failure and strain rate effect into consideration.A good agreement between the experimental observations and numerical results is achieved to prove the validity of the modelling method.The tests and simulations show that the impact-induced deformation on the human body is significantly reduced by using STG-modified EVA as the buffering material.The improvement of protective performance is attributed to better dynamic properties and more outstanding energy absorption capability of the composite foam.展开更多
Tungsten nanoparticle-strengthened Cu composites were prepared from nanopowder synthesized by a sol–gel method and in-situ hydrogen reduction.The tungsten particles in the Cu matrix were well-dispersed with an averag...Tungsten nanoparticle-strengthened Cu composites were prepared from nanopowder synthesized by a sol–gel method and in-situ hydrogen reduction.The tungsten particles in the Cu matrix were well-dispersed with an average size of approximately 100–200 nm.The addition of nanosized W particles remarkably improves the mechanical properties,while the electrical conductivity did not substantially decrease.The Cu–W composite with 6 wt%W has the most comprehensive properties with an ultimate strength of 310 MPa,yield strength of 238 MPa,hardness of HV 108 and electrical conductivity of 90%IACS.The enhanced mechanical property and only a small loss of electrical conductivity demonstrate the potential of this new strategy to prepare W nanoparticle-strengthened Cu composites.展开更多
Bone-like nanohydroxyapatite powders (b-nanoHA) were synthesized in simulated body fluid (SBF). The b-nanoHA, gelatin (Gel) and Polyvinyl Alcohol (PVA) were used to prepare bone-like composites (b-nanoHA/ Gel/PVA) at ...Bone-like nanohydroxyapatite powders (b-nanoHA) were synthesized in simulated body fluid (SBF). The b-nanoHA, gelatin (Gel) and Polyvinyl Alcohol (PVA) were used to prepare bone-like composites (b-nanoHA/ Gel/PVA) at room temperature. Characterizations of b-nanoHA powders and b-nanoHA/Gel/PVA composites were investigated by using X-ray diffraction (XRD), transmission electron microscopy (TEM), High-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). Bending strength and compressive strength of the composite were tested. It was found that microstructure of the b-nanoHA powders was whisker shape and its crystalline degree was low similar to natural bone, bending strength and compressive strength of the b-nanoHA/Gel/PVA composite depended on the mixing ratio of HA, Gel and PVA, and also PVA could induce the network formation in the b-nanoHA/Gel/ PVA composite.展开更多
Cu(NO3)2 and (NH4)6H2W12O40?4H2O were used to prepare W/Cu nanosized composite powder by sol-gel tech-nique. The influences of heat treatment process, pH value of the solution and the amount of an addition agent on pa...Cu(NO3)2 and (NH4)6H2W12O40?4H2O were used to prepare W/Cu nanosized composite powder by sol-gel tech-nique. The influences of heat treatment process, pH value of the solution and the amount of an addition agent on particle size were investigated by DSC, XRD and TEM. The results show that, at a certain heat treatment temperature, the W/Cu nanoparticle size increases with the pH value or the amount of the addition agent increasing.展开更多
A composite gel was prepared for plugging CO2 channeling, which is a serious problem for enhanced oil recovery with CO2. A composite gel which is one of the materials for successful control of CO2 channeling during CO...A composite gel was prepared for plugging CO2 channeling, which is a serious problem for enhanced oil recovery with CO2. A composite gel which is one of the materials for successful control of CO2 channeling during CO2 injection process was studied in this paper. SEM and nano particle size analysis were used to describe this material’s microstructure. Its effect on CO2 channeling control was evaluated with core flow experiments. Both the rheological test and core plugging experiments indicated that both acrylamide monomer concentration and reaction pressure had positive influences on gel properties. The gel system with an acrylamide monomer concentration of 2% and 5% sodium silicate was proved to have excellent strength, elastic and plugging efficiency, which confirmed huge development potential and wide application of the composite gel system. The high-pressure acid environment arising from the CO2 injection not only reacts with solid silicate to form silicic acid gel, but also facilitates efficient polymerization.展开更多
SiC-Al2O3 composite powder was prepared by sol-gel and carbothermal reduction method. The powder synthesized was characterized by X-ray diffraction(XRD) and scanning electron microscopy(SEM) to confirm the phase forma...SiC-Al2O3 composite powder was prepared by sol-gel and carbothermal reduction method. The powder synthesized was characterized by X-ray diffraction(XRD) and scanning electron microscopy(SEM) to confirm the phase formation, and the thermodynamic analysis was performed systematically. Moreover, the variation of its microwave permittivity with different atomic ratio of Al/Si was investigated in the frequency range of 8.2-12.4 GHz. The results show that, the powder obtained consists of spherical particles of 300-400 nm in diameter, which are composed of SiC and Al2O3 microcrystal with the grain size of approximately 45 nm. The results of XRD accord with those of the thermodynamic analysis. It is impossible for Al atoms to dissolve in the lattice of SiC during the carbothermal reduction process. Along with the increase of atomic ratio of Al/Si in the xerogel, the amount of Al2O3 in the powder synthesized increases, which reduces bothε', the real part of complex permittivity, and tgδ(ε'/ε'), the dissipation factor, whereε' is the imaginary part of complex permittivity.展开更多
A LiFePO4/(C+Fe2P) composite cathode material was prepared by a sol-gel method using Fe(NO3)3·9H2O,LiAc·H2O,NH4H2PO4 and citric acid as raw materials,and the physical properties and electrochemical performan...A LiFePO4/(C+Fe2P) composite cathode material was prepared by a sol-gel method using Fe(NO3)3·9H2O,LiAc·H2O,NH4H2PO4 and citric acid as raw materials,and the physical properties and electrochemical performance of the composite cathode material were investigated by X-ray diffractometry(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM) and electrochemical tests.The Fe2P content,morphology and electrochemical performance of LiFePO4/(C+Fe2P) composite depend on the calcination temperature.The optimized LiFePO4/(C+Fe2P) composite is prepared at 650 °C and the optimized composite exhibits sphere-like morphology with porous structure and Fe2P content of about 3.2%(mass fraction).The discharge capacity of the optimized LiFePO4/(C+Fe2P) at 0.1C is 156 and 161 mA·h/g at 25 and 55 °C,respectively,and the corresponding capacity retentions are 96% after 30 cycles;while the capacity at 1C is 142 and 149 mA·h/g at 25 and 55 °C,respectively,and the capacity still remains 135 and 142 mA·h/g after 30 cycles at 25 and 55 °C,respectively.展开更多
Composite polymer electrolytes based on polyethylene oxide(PEO) were prepared by using LiClO4 as doping salt and silane-modified SiO2 as filler. SiO2 was formed in-situ in (PEO)8LiClO4 matrix by the hydrolysis and con...Composite polymer electrolytes based on polyethylene oxide(PEO) were prepared by using LiClO4 as doping salt and silane-modified SiO2 as filler. SiO2 was formed in-situ in (PEO)8LiClO4 matrix by the hydrolysis and condensation reaction of Si(OC4H9)4. The crystallinity,morphology and ionic conductivity of composite polymer electrolyte films were examined by differential scanning calorimetry,scanning electron microscopy,atom force microscopy and alternating current impedance spectroscopy,respectively. Compared with the crystallinity of the unmodified SiO2 as inert filler,that of composite polymer electrolytes is decreased. The results show that silane-modified SiO2 particles are uniformly dispersed in (PEO)8LiClO4 composite polymer electrolyte film and the addition of silane-modified SiO2 increases the ionic conductivity of the (PEO)8LiClO4 more noticeably. When the mass fraction of SiO2 is about 10%,the conductivity of (PEO)8LiClO4-modified SiO2 attains a maximum value of 4.8×10-5 S·cm-1.展开更多
In this study,the sol-gel method was introduced to prepare the composite phase change material (CPCM). The CPCM was added to fabric with coating techniques and the thermal activity of modified fabric was studied. In a...In this study,the sol-gel method was introduced to prepare the composite phase change material (CPCM). The CPCM was added to fabric with coating techniques and the thermal activity of modified fabric was studied. In addition,the thermal property and the microstructure of CPCM were also discussed in detail by means of polarization microscope and differential scanning calorimeter,respectively. According to the analysis of main influencial factors of the property of CPCM,the optimal preparing technique was determined. It was proved that CPCM could exhibit a good thermal property while phase transformation process took place,and a better appearance of the fabric modified with CPCM could be obtained due to the fact that in a warm circumstance,the liquid-state phase change material could be firmly enwrapped and embedded in the three-dimensional network all the time during the phase transformation. Besides,the fabric treated with CPCM had a high phase-transition enthalpy and an appropriate phase-transition temperature. As a result,a desirable temperature-adjustable function appeared.展开更多
This article presents a detailed structural study of a new spherical Mg Cl2-supported Ti Cl4 Ziegler-Natta catalyst for isotactic propylene polymerization, and researches on the relationship between catalyst structure...This article presents a detailed structural study of a new spherical Mg Cl2-supported Ti Cl4 Ziegler-Natta catalyst for isotactic propylene polymerization, and researches on the relationship between catalyst structure and polymer properties. The spherical support with the chemical composition of CH3CH2 OMg OCH(CH2Cl)2 has been synthesized from a new dispersion system and is used as the supporting material to prepare Ziegler-Natta catalyst. The XRD analysis indicates that the catalyst is fully activated with δ-Mg Cl2 in the active catalyst. The far-IR spectrometric results confirm again the presence of δ-Mg Cl2 in the active catalyst. Textural property of the active catalyst exhibits high surface area coupled with high porosity. The high activity in propylene polymerization is mainly ascribed to the full activation and the porous structure of the catalyst. Scanning electron microscopy/energy dispersive spectrometer mapping results indicate a uniform titanium distribution throughout the catalyst particles. Particle size analysis shows that the catalyst has a narrow particle size distribution. The perfect spherical shape, uniform titanium distribution and narrow particle size distribution of the catalyst confirm the advantage of polymer particles production with less fines. The solid state 13 C NMR and mid-IR spectroscopic analyses indicate that there exists strong complexation between diisobutyl phthalate and Mg Cl2, which leads to the high isotacticity of polypropylene.展开更多
SnO2-Li4Ti5O12 was prepared by sol-gel method using tin tetrachloride,lithium acetate,tetrabutylorthotitanate and aqueous ammonia as starting materials.The composite was characterized by thermogravimertric(TG)analysis...SnO2-Li4Ti5O12 was prepared by sol-gel method using tin tetrachloride,lithium acetate,tetrabutylorthotitanate and aqueous ammonia as starting materials.The composite was characterized by thermogravimertric(TG)analysis and differential thermal analysis(DTA),X-ray diffractometry(XRD)and transmission electron microscopy(TEM)combined with electrochemical tests.The results show that SnO2-Li4Ti5O12 composite derived by sol-gel technique is a nanocomposite with core-shell structure, and the amorphous Li4Ti5O12 layer with 20?40 nm in thickness is coated on the surface of SnO2 particles.Electrochemical tests show that SnO2-Li4Ti5O12 composite delivers a reversible capacity of 688.7 mA·h/g at 0.1C and 93.4%of that is retained after 60 cycles at 0.2C.The amorphous Li4Ti5O12 in composite can accommodate the volume change of SnO2 electrode and prevent the small and active Sn particles from aggregating into larger and inactive Sn clusters during the cycling effectively,and enhance the cycling stability of SnO2 electrode significantly.展开更多
In the presence of titanium dioxide powder, cross-linking reaction between commercial polyvinyl alcohol(PVA)-based macromonomer and acrylic acid(AA) was initiated with potassium persulfate in an emulsifying system. As...In the presence of titanium dioxide powder, cross-linking reaction between commercial polyvinyl alcohol(PVA)-based macromonomer and acrylic acid(AA) was initiated with potassium persulfate in an emulsifying system. As a result, PVA-AA/TiO2 composite gel particles were obtained. The morphology and composition of the particles were analyzed with scanning electron microscopy(SEM), energy scattering x-ray spectroscopy(EDS), Fourier infrared spectroscopy(FTIR), and thermogravimetric analysis(TGA). The analysis results confirmed that the particles were the expected ones. TiO2 was dispersed homogeneously within the spheroidal particles. Compared to the control gel, the composite gel particles not only contained Ti element but also showed higher thermal stability. In addition, the photo-catalytic behavior of the particles for the degradation of methyl orange contained in aqueous solution was examined. The particles exhibited photocatalytic characteristic for the degradation of the model dye, which could be modulated by simply varying the amount of cross-linking agent or TiO2. The photo-catalytic degradation percentage of methyl orange maintained at 91%-96% after using the particles three times, which indicated that TiO2 could played its role repeatedly via being fixated within polyvinyl alcohol-based gel.展开更多
An Al2O3 protective coating on magnesium alloy AZ31 was prepared by a repeated direct sol-gel process annealing at 300℃and a composite coating was also deposited using Al2O3 particles dispersed sol followed by phosph...An Al2O3 protective coating on magnesium alloy AZ31 was prepared by a repeated direct sol-gel process annealing at 300℃and a composite coating was also deposited using Al2O3 particles dispersed sol followed by phosphating treatment and annealing at 300℃.The morphologies,structures and critical adhesive loads as well as corrosion properties of the coatings were comparatively investigated by scanning electron microscopy(SEM),X-ray diffractometry(XRD),nanoscratch test and electrochemical measurement.The results show that the composite coating has a more uniform,crack-free layer and improved adhesion to the substrate as compared with that of the repeated direct sol-gel coating owing to its lower heat strain.The main phases in both coatings consist ofγ-Al2O3 andδ-Al2O3 derived from annealed alumina sol,and the composite coating has an anticorrosion performance which is superior to that of the repeated direct sol-gel coating.展开更多
The supported membranes of Al 2O 3 and its modification membranes were prepared.Al 2O 3,Al 2O 3 SiO 2 TiO 2 and Al 2O 3 SiO 2 TiO 2 ZrO 2 membranes were mamufatured by the slip casting process using mixing boehmite,si...The supported membranes of Al 2O 3 and its modification membranes were prepared.Al 2O 3,Al 2O 3 SiO 2 TiO 2 and Al 2O 3 SiO 2 TiO 2 ZrO 2 membranes were mamufatured by the slip casting process using mixing boehmite,silicate,titania and zirconia sols under proper conditions,then the composite membrane was prepared.The structure and characteristics of the membrane were determined by XRD,SEM and AFM measurement.The conditions of preparation of the membrane are discussed.The thickness of the layer is about 1-2μm,the diameter of an average pore is 200-300nm and has a narrow pore distribution without crack forming.By changing the ratios of Al∶Si∶Ti∶Zr(mol),variations of surface pore size of Al 2O 3 SiO 2 TiO 2 ZrO 2 membrane can be gained.展开更多
Graphite/TiO2 composite particles were obtained by sol-gel technique in this paper. The structure and characteristic of the composite particles are analyzed by XRD, SEM and TG-DTA. The electrorheological properties of...Graphite/TiO2 composite particles were obtained by sol-gel technique in this paper. The structure and characteristic of the composite particles are analyzed by XRD, SEM and TG-DTA. The electrorheological properties of the ER fluid containing the particles were measured by a Couette-type rheometer under shear rates of 1～136 s-1 and AC electric fields of 0～3 kV/mm. The experimental results show that the leaking current density of the ER fluid is higher than that of pure titanium dioxide particles dispersed in damping oil. The shear yield stress of the ER fluid increases with increasing electric field and exhibits a typical Bingham flow behavior. The suspension demonstrates an excellent ER performance (τ/τ0=1200) compared with conventional ER fluids (τ/τ0 ≤500). The sedimentation of the ER fluid is improved obviously due to the coating effect of the particles.展开更多
Nano-hydroxyapatite reinforced poly(vinyl alcohol) gel(nano-HA/PVA gel) composites has been proposed as a promising biomaterial,especially used as an articular cartilage repair biomaterial.In this paper,nano-HA/PVA ge...Nano-hydroxyapatite reinforced poly(vinyl alcohol) gel(nano-HA/PVA gel) composites has been proposed as a promising biomaterial,especially used as an articular cartilage repair biomaterial.In this paper,nano-HA/PVA gel composite was prepared by in situ synthesis method and incorporation with freeze-thaw cycle process.The microstructure and morphology were investigated by X-ray diffraction,TEM,SEM and FTIR.The results showed that the size of HA particles synthesized in PVA solution was on the nanometer scale.Both the size and crystallinity of HA particles synthesized in PVA solution decreased compared with that of HA synthesized in distilled water.The nano-HA particles were distributed in PVA matrix uniformly due to the effect of PVA solution as a dispersant while low content of HA particles in the composites.On the contrary,with high content of nano-HA particles in the composites,the particles tended to aggregate.The result of FT-IR analysis indicated that the chemical bond between nano-HA particles and PVA matrix existed.The conformation and degree of tacticity of PVA molecule changed because of the addition of HA particles.Furthermore,the interfacial strength of the composites was improved due to the interaction between nano-HA particle and PVA matrix and this was beneficial to improving the mechanical properties of the composites.展开更多
The composite films consisting of the titania gel impregnated with hydroxyapatite (HAP) submicron particles were prepared on commercial Ti6Al4V plates processed by a sol-gel route. HAP powders were synthesized based o...The composite films consisting of the titania gel impregnated with hydroxyapatite (HAP) submicron particles were prepared on commercial Ti6Al4V plates processed by a sol-gel route. HAP powders were synthesized based on wet chemical precipitation method with Ca(NO3)2·4H2O and (NH4)2HPO4 as starting reagents. After being calcined at 900°C,HAP powders were ultrasonically scattered in ethanol to produce HAP sol. The titania sol was prepared using titanium (IV) isopropoxide {Ti[OCH(CH3)2]4} as precursor. Both the titania sol and the HAP/titania mixture were sequentially spin-coated on the substrates and calcined at various temperatures. The characteristics and mechanical adhesion of the composite films were investigated. The results show that the as-prepared films are dense,homogeneous,well-crystallized,and there is a good interfacial adhesion between the film and the substrate. The in vitro bioac-tivities of these films were discussed based on the analysis of the variations of Ca and P concentrations in the simulated body fluid and their surface morphologies against immersion time.展开更多
Photocatalyst of TiO2 bonded active carbon （TiO2/AC）, was prepared via sol-gel method from a mixture of TiO2 sol with active carbon. Post heat treatment was performed at 250 ℃ for 2 h in air and then kept at 400 ℃...Photocatalyst of TiO2 bonded active carbon （TiO2/AC）, was prepared via sol-gel method from a mixture of TiO2 sol with active carbon. Post heat treatment was performed at 250 ℃ for 2 h in air and then kept at 400 ℃ to 600 ℃ under a flow of nitrogen for 2 h. The TiO2/AC composites obtained were characterized by SEM, XRD, UV-vis and BET. The photocatalytic activities of the TiO2/AC composites were studied in comparison with TiO2, AC, P-25 and a mixture of TiO2 and AC, respectively. The Ramnant rate of Rhodamine B absorbed by the active carbon is found to be almost 70% and the remnant rates of the Rhodamine B decolorized by TiO2 and the mixture of TiO2 and the active carbon are 30% and 25%, respectively. However, nearly complete removal of Rhodamine B is observed for a TiO2/AC composite after 200 min under UV irradiation, which will take the P-25 commercial product 5 h. Therefore, the TiO2/AC composite is much more effective in decolorization of aqueous Rhodamine B. In addition, the composite can be easily separated from solutions.展开更多
Barium strontium titanate (Ba 0.5 Sr 0.5 TiO 3 , BST)/silicon nanoporous pillar array (Si-NPA) thin films were prepared by a spin-coating/annealing technique based on Si-NPA with micro/nano-structure. Both the isomer ...Barium strontium titanate (Ba 0.5 Sr 0.5 TiO 3 , BST)/silicon nanoporous pillar array (Si-NPA) thin films were prepared by a spin-coating/annealing technique based on Si-NPA with micro/nano-structure. Both the isomer conversion of acetylacetone and the network structure combined by enol and Ti-alkoxide facilitate the formation of the BST sol and the subsequent crystallization. Before the perovskite BST begins to form, the intermediate phase (Ba,Sr)Ti 2 O 5 CO 3 is found. The boundary between BST and Si-NPA is of clarity and little interface diffusion, disclosing that Si-NPA is an ideal template substrate in the preparation of multifunctional composite films.展开更多
基金Funded by the National Natural Science Foundation of China(No.51678254)。
文摘Gypsum was used as substrate,and silica gel was mixed into substrate at a certain mass ratio to prepare humidity-controlling composites;moreover,the moisture absorption and desorption properties of gypsum-based composites were compared with adding different silica gel particle size and proportion.The morphological characteristics,the isothermal equilibrium moisture content curve,moisture absorption and desorption rate,moisture absorption and desorption stability,and humidity-conditioning performance were tested and analyzed.The experimental results show that,compared with pure-gypsum,the surface structure of the gypsum-based composites is relatively loose,the quantity,density and aperture of the pores in the structure increase.The absorption and desorption capacity increase along with the increase of silica gel particle size and silica gel proportion.When 3 mm silica gel particle size is added with a mass ratio of 40%,the maximum equilibrium moisture content of humidity-controlling composites is 0.161 g/g at 98% relative humidity(RH),3.22 times that of pure-gypsum.The moisture absorption and desorption rates are increased,the equilibrium moisture absorption and desorption rates are 2.68 times and 1.61 times that of pure-gypsum at 58.5% RH,respectively.The gypsum-based composites have a good stability,which has better timely response to dynamic humidity changes and can effectively regulate indoor humidity under natural conditions.
基金the National Natural Science Foundation of China(Grant Nos.12072356 and 12232020)the Science and Technology on Transient Impact Laboratory(Grant No.6142606221105)the Beijing Municipal Science and Technology Commission(Grant No.Z221100005822006).
文摘As one of the most widely used personal protective equipment(PPE),body armors play an important role in protecting the human body from the high-velocity impact of bullets or projectiles.The body torso and critical organs of the wear may suffer severe behind-armor blunt trauma(BABT)even though the impactor is stopped by the body armor.A type of novel composite material through incorporating shear stiffening gel(STG)into ethylene-vinyl acetate(EVA)foam is developed and used as buffer layers to reduce BABT.In this paper,the protective performance of body armors composed of fabric bulletproof layers and a buffer layer made of foam material is investigated both experimentally and numerically.The effectiveness of STG-modified EVA in damage relief is verified by ballistic tests.In parallel with the experimental study,numerical simulations are conducted by LS-DYNA®to investigate the dynamic response of each component and capture the key mechanical parameters,which are hardly obtained from field tests.To fully describe the material behavior under the transient impact,the selected constitutive models take the failure and strain rate effect into consideration.A good agreement between the experimental observations and numerical results is achieved to prove the validity of the modelling method.The tests and simulations show that the impact-induced deformation on the human body is significantly reduced by using STG-modified EVA as the buffering material.The improvement of protective performance is attributed to better dynamic properties and more outstanding energy absorption capability of the composite foam.
基金supported by the Fundamental Research Funds for the Central Universities (No. FRF-TP-18-029A2)State Key Lab of Advanced Metals and Materials of China (No. 2019-Z10)
文摘Tungsten nanoparticle-strengthened Cu composites were prepared from nanopowder synthesized by a sol–gel method and in-situ hydrogen reduction.The tungsten particles in the Cu matrix were well-dispersed with an average size of approximately 100–200 nm.The addition of nanosized W particles remarkably improves the mechanical properties,while the electrical conductivity did not substantially decrease.The Cu–W composite with 6 wt%W has the most comprehensive properties with an ultimate strength of 310 MPa,yield strength of 238 MPa,hardness of HV 108 and electrical conductivity of 90%IACS.The enhanced mechanical property and only a small loss of electrical conductivity demonstrate the potential of this new strategy to prepare W nanoparticle-strengthened Cu composites.
文摘Bone-like nanohydroxyapatite powders (b-nanoHA) were synthesized in simulated body fluid (SBF). The b-nanoHA, gelatin (Gel) and Polyvinyl Alcohol (PVA) were used to prepare bone-like composites (b-nanoHA/ Gel/PVA) at room temperature. Characterizations of b-nanoHA powders and b-nanoHA/Gel/PVA composites were investigated by using X-ray diffraction (XRD), transmission electron microscopy (TEM), High-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). Bending strength and compressive strength of the composite were tested. It was found that microstructure of the b-nanoHA powders was whisker shape and its crystalline degree was low similar to natural bone, bending strength and compressive strength of the b-nanoHA/Gel/PVA composite depended on the mixing ratio of HA, Gel and PVA, and also PVA could induce the network formation in the b-nanoHA/Gel/ PVA composite.
基金This Project was financially supported by the National Natural Science Foundation of China (No. 50471033).
文摘Cu(NO3)2 and (NH4)6H2W12O40?4H2O were used to prepare W/Cu nanosized composite powder by sol-gel tech-nique. The influences of heat treatment process, pH value of the solution and the amount of an addition agent on particle size were investigated by DSC, XRD and TEM. The results show that, at a certain heat treatment temperature, the W/Cu nanoparticle size increases with the pH value or the amount of the addition agent increasing.
文摘A composite gel was prepared for plugging CO2 channeling, which is a serious problem for enhanced oil recovery with CO2. A composite gel which is one of the materials for successful control of CO2 channeling during CO2 injection process was studied in this paper. SEM and nano particle size analysis were used to describe this material’s microstructure. Its effect on CO2 channeling control was evaluated with core flow experiments. Both the rheological test and core plugging experiments indicated that both acrylamide monomer concentration and reaction pressure had positive influences on gel properties. The gel system with an acrylamide monomer concentration of 2% and 5% sodium silicate was proved to have excellent strength, elastic and plugging efficiency, which confirmed huge development potential and wide application of the composite gel system. The high-pressure acid environment arising from the CO2 injection not only reacts with solid silicate to form silicic acid gel, but also facilitates efficient polymerization.
基金Project (50572090) supported by the National Natural Science Foundation of China
文摘SiC-Al2O3 composite powder was prepared by sol-gel and carbothermal reduction method. The powder synthesized was characterized by X-ray diffraction(XRD) and scanning electron microscopy(SEM) to confirm the phase formation, and the thermodynamic analysis was performed systematically. Moreover, the variation of its microwave permittivity with different atomic ratio of Al/Si was investigated in the frequency range of 8.2-12.4 GHz. The results show that, the powder obtained consists of spherical particles of 300-400 nm in diameter, which are composed of SiC and Al2O3 microcrystal with the grain size of approximately 45 nm. The results of XRD accord with those of the thermodynamic analysis. It is impossible for Al atoms to dissolve in the lattice of SiC during the carbothermal reduction process. Along with the increase of atomic ratio of Al/Si in the xerogel, the amount of Al2O3 in the powder synthesized increases, which reduces bothε', the real part of complex permittivity, and tgδ(ε'/ε'), the dissipation factor, whereε' is the imaginary part of complex permittivity.
基金Project(50571091) supported by the National Natural Science Foundation of ChinaProject(09C947) supported by the Scientific Research Fund of Hunan Provincial Education Department,China
文摘A LiFePO4/(C+Fe2P) composite cathode material was prepared by a sol-gel method using Fe(NO3)3·9H2O,LiAc·H2O,NH4H2PO4 and citric acid as raw materials,and the physical properties and electrochemical performance of the composite cathode material were investigated by X-ray diffractometry(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM) and electrochemical tests.The Fe2P content,morphology and electrochemical performance of LiFePO4/(C+Fe2P) composite depend on the calcination temperature.The optimized LiFePO4/(C+Fe2P) composite is prepared at 650 °C and the optimized composite exhibits sphere-like morphology with porous structure and Fe2P content of about 3.2%(mass fraction).The discharge capacity of the optimized LiFePO4/(C+Fe2P) at 0.1C is 156 and 161 mA·h/g at 25 and 55 °C,respectively,and the corresponding capacity retentions are 96% after 30 cycles;while the capacity at 1C is 142 and 149 mA·h/g at 25 and 55 °C,respectively,and the capacity still remains 135 and 142 mA·h/g after 30 cycles at 25 and 55 °C,respectively.
文摘Composite polymer electrolytes based on polyethylene oxide(PEO) were prepared by using LiClO4 as doping salt and silane-modified SiO2 as filler. SiO2 was formed in-situ in (PEO)8LiClO4 matrix by the hydrolysis and condensation reaction of Si(OC4H9)4. The crystallinity,morphology and ionic conductivity of composite polymer electrolyte films were examined by differential scanning calorimetry,scanning electron microscopy,atom force microscopy and alternating current impedance spectroscopy,respectively. Compared with the crystallinity of the unmodified SiO2 as inert filler,that of composite polymer electrolytes is decreased. The results show that silane-modified SiO2 particles are uniformly dispersed in (PEO)8LiClO4 composite polymer electrolyte film and the addition of silane-modified SiO2 increases the ionic conductivity of the (PEO)8LiClO4 more noticeably. When the mass fraction of SiO2 is about 10%,the conductivity of (PEO)8LiClO4-modified SiO2 attains a maximum value of 4.8×10-5 S·cm-1.
基金Fujian Province I mportant Science and Technology Development Fund,China (No.2005Z17)
文摘In this study,the sol-gel method was introduced to prepare the composite phase change material (CPCM). The CPCM was added to fabric with coating techniques and the thermal activity of modified fabric was studied. In addition,the thermal property and the microstructure of CPCM were also discussed in detail by means of polarization microscope and differential scanning calorimeter,respectively. According to the analysis of main influencial factors of the property of CPCM,the optimal preparing technique was determined. It was proved that CPCM could exhibit a good thermal property while phase transformation process took place,and a better appearance of the fabric modified with CPCM could be obtained due to the fact that in a warm circumstance,the liquid-state phase change material could be firmly enwrapped and embedded in the three-dimensional network all the time during the phase transformation. Besides,the fabric treated with CPCM had a high phase-transition enthalpy and an appropriate phase-transition temperature. As a result,a desirable temperature-adjustable function appeared.
基金the financial support by the National Natural Science Foundation of China (No. 20973022 and No. 11472048)
文摘This article presents a detailed structural study of a new spherical Mg Cl2-supported Ti Cl4 Ziegler-Natta catalyst for isotactic propylene polymerization, and researches on the relationship between catalyst structure and polymer properties. The spherical support with the chemical composition of CH3CH2 OMg OCH(CH2Cl)2 has been synthesized from a new dispersion system and is used as the supporting material to prepare Ziegler-Natta catalyst. The XRD analysis indicates that the catalyst is fully activated with δ-Mg Cl2 in the active catalyst. The far-IR spectrometric results confirm again the presence of δ-Mg Cl2 in the active catalyst. Textural property of the active catalyst exhibits high surface area coupled with high porosity. The high activity in propylene polymerization is mainly ascribed to the full activation and the porous structure of the catalyst. Scanning electron microscopy/energy dispersive spectrometer mapping results indicate a uniform titanium distribution throughout the catalyst particles. Particle size analysis shows that the catalyst has a narrow particle size distribution. The perfect spherical shape, uniform titanium distribution and narrow particle size distribution of the catalyst confirm the advantage of polymer particles production with less fines. The solid state 13 C NMR and mid-IR spectroscopic analyses indicate that there exists strong complexation between diisobutyl phthalate and Mg Cl2, which leads to the high isotacticity of polypropylene.
基金Project(20873054)supported by the National Natural Science Foundation of ChinaProject(2005037700)supported by Postdoctoral Science Foundation of China+2 种基金Project(07JJ3014)supported by Hunan Provincial Natural Science Foundation of ChinaProject(07A058)supported by Scientific Research Fund of Hunan Provincial Education DepartmentProject(2004107)supported by Postdoctoral Science Foundation of Central South University
文摘SnO2-Li4Ti5O12 was prepared by sol-gel method using tin tetrachloride,lithium acetate,tetrabutylorthotitanate and aqueous ammonia as starting materials.The composite was characterized by thermogravimertric(TG)analysis and differential thermal analysis(DTA),X-ray diffractometry(XRD)and transmission electron microscopy(TEM)combined with electrochemical tests.The results show that SnO2-Li4Ti5O12 composite derived by sol-gel technique is a nanocomposite with core-shell structure, and the amorphous Li4Ti5O12 layer with 20?40 nm in thickness is coated on the surface of SnO2 particles.Electrochemical tests show that SnO2-Li4Ti5O12 composite delivers a reversible capacity of 688.7 mA·h/g at 0.1C and 93.4%of that is retained after 60 cycles at 0.2C.The amorphous Li4Ti5O12 in composite can accommodate the volume change of SnO2 electrode and prevent the small and active Sn particles from aggregating into larger and inactive Sn clusters during the cycling effectively,and enhance the cycling stability of SnO2 electrode significantly.
基金Funded by the Science&Technology Program of Fujian Province(No.2017H0018)
文摘In the presence of titanium dioxide powder, cross-linking reaction between commercial polyvinyl alcohol(PVA)-based macromonomer and acrylic acid(AA) was initiated with potassium persulfate in an emulsifying system. As a result, PVA-AA/TiO2 composite gel particles were obtained. The morphology and composition of the particles were analyzed with scanning electron microscopy(SEM), energy scattering x-ray spectroscopy(EDS), Fourier infrared spectroscopy(FTIR), and thermogravimetric analysis(TGA). The analysis results confirmed that the particles were the expected ones. TiO2 was dispersed homogeneously within the spheroidal particles. Compared to the control gel, the composite gel particles not only contained Ti element but also showed higher thermal stability. In addition, the photo-catalytic behavior of the particles for the degradation of methyl orange contained in aqueous solution was examined. The particles exhibited photocatalytic characteristic for the degradation of the model dye, which could be modulated by simply varying the amount of cross-linking agent or TiO2. The photo-catalytic degradation percentage of methyl orange maintained at 91%-96% after using the particles three times, which indicated that TiO2 could played its role repeatedly via being fixated within polyvinyl alcohol-based gel.
基金Project(2005Z023)supported by the Scientific Research Initial Funding of Chongqing University of Technology
文摘An Al2O3 protective coating on magnesium alloy AZ31 was prepared by a repeated direct sol-gel process annealing at 300℃and a composite coating was also deposited using Al2O3 particles dispersed sol followed by phosphating treatment and annealing at 300℃.The morphologies,structures and critical adhesive loads as well as corrosion properties of the coatings were comparatively investigated by scanning electron microscopy(SEM),X-ray diffractometry(XRD),nanoscratch test and electrochemical measurement.The results show that the composite coating has a more uniform,crack-free layer and improved adhesion to the substrate as compared with that of the repeated direct sol-gel coating owing to its lower heat strain.The main phases in both coatings consist ofγ-Al2O3 andδ-Al2O3 derived from annealed alumina sol,and the composite coating has an anticorrosion performance which is superior to that of the repeated direct sol-gel coating.
基金Project cooperated with College of Environment Engineering,Huazhong University of Technology
文摘The supported membranes of Al 2O 3 and its modification membranes were prepared.Al 2O 3,Al 2O 3 SiO 2 TiO 2 and Al 2O 3 SiO 2 TiO 2 ZrO 2 membranes were mamufatured by the slip casting process using mixing boehmite,silicate,titania and zirconia sols under proper conditions,then the composite membrane was prepared.The structure and characteristics of the membrane were determined by XRD,SEM and AFM measurement.The conditions of preparation of the membrane are discussed.The thickness of the layer is about 1-2μm,the diameter of an average pore is 200-300nm and has a narrow pore distribution without crack forming.By changing the ratios of Al∶Si∶Ti∶Zr(mol),variations of surface pore size of Al 2O 3 SiO 2 TiO 2 ZrO 2 membrane can be gained.
基金The authors are thankful to the support of the National Natural Science Foundation of China(Grant No.50135030).
文摘Graphite/TiO2 composite particles were obtained by sol-gel technique in this paper. The structure and characteristic of the composite particles are analyzed by XRD, SEM and TG-DTA. The electrorheological properties of the ER fluid containing the particles were measured by a Couette-type rheometer under shear rates of 1～136 s-1 and AC electric fields of 0～3 kV/mm. The experimental results show that the leaking current density of the ER fluid is higher than that of pure titanium dioxide particles dispersed in damping oil. The shear yield stress of the ER fluid increases with increasing electric field and exhibits a typical Bingham flow behavior. The suspension demonstrates an excellent ER performance (τ/τ0=1200) compared with conventional ER fluids (τ/τ0 ≤500). The sedimentation of the ER fluid is improved obviously due to the coating effect of the particles.
基金Funded by the Natural Science Research of Key Projects of Anhui Provincial Universities (No. KJ2010A099)
文摘Nano-hydroxyapatite reinforced poly(vinyl alcohol) gel(nano-HA/PVA gel) composites has been proposed as a promising biomaterial,especially used as an articular cartilage repair biomaterial.In this paper,nano-HA/PVA gel composite was prepared by in situ synthesis method and incorporation with freeze-thaw cycle process.The microstructure and morphology were investigated by X-ray diffraction,TEM,SEM and FTIR.The results showed that the size of HA particles synthesized in PVA solution was on the nanometer scale.Both the size and crystallinity of HA particles synthesized in PVA solution decreased compared with that of HA synthesized in distilled water.The nano-HA particles were distributed in PVA matrix uniformly due to the effect of PVA solution as a dispersant while low content of HA particles in the composites.On the contrary,with high content of nano-HA particles in the composites,the particles tended to aggregate.The result of FT-IR analysis indicated that the chemical bond between nano-HA particles and PVA matrix existed.The conformation and degree of tacticity of PVA molecule changed because of the addition of HA particles.Furthermore,the interfacial strength of the composites was improved due to the interaction between nano-HA particle and PVA matrix and this was beneficial to improving the mechanical properties of the composites.
基金This work was financially supported by the National Natural Science Foundation of China (No.50235020).
文摘The composite films consisting of the titania gel impregnated with hydroxyapatite (HAP) submicron particles were prepared on commercial Ti6Al4V plates processed by a sol-gel route. HAP powders were synthesized based on wet chemical precipitation method with Ca(NO3)2·4H2O and (NH4)2HPO4 as starting reagents. After being calcined at 900°C,HAP powders were ultrasonically scattered in ethanol to produce HAP sol. The titania sol was prepared using titanium (IV) isopropoxide {Ti[OCH(CH3)2]4} as precursor. Both the titania sol and the HAP/titania mixture were sequentially spin-coated on the substrates and calcined at various temperatures. The characteristics and mechanical adhesion of the composite films were investigated. The results show that the as-prepared films are dense,homogeneous,well-crystallized,and there is a good interfacial adhesion between the film and the substrate. The in vitro bioac-tivities of these films were discussed based on the analysis of the variations of Ca and P concentrations in the simulated body fluid and their surface morphologies against immersion time.
文摘Photocatalyst of TiO2 bonded active carbon （TiO2/AC）, was prepared via sol-gel method from a mixture of TiO2 sol with active carbon. Post heat treatment was performed at 250 ℃ for 2 h in air and then kept at 400 ℃ to 600 ℃ under a flow of nitrogen for 2 h. The TiO2/AC composites obtained were characterized by SEM, XRD, UV-vis and BET. The photocatalytic activities of the TiO2/AC composites were studied in comparison with TiO2, AC, P-25 and a mixture of TiO2 and AC, respectively. The Ramnant rate of Rhodamine B absorbed by the active carbon is found to be almost 70% and the remnant rates of the Rhodamine B decolorized by TiO2 and the mixture of TiO2 and the active carbon are 30% and 25%, respectively. However, nearly complete removal of Rhodamine B is observed for a TiO2/AC composite after 200 min under UV irradiation, which will take the P-25 commercial product 5 h. Therefore, the TiO2/AC composite is much more effective in decolorization of aqueous Rhodamine B. In addition, the composite can be easily separated from solutions.
基金supported by the Research Funds of Guangxi Key Laboratory of Information Materials, China (No.0710908-04-K)Guangxi Natural Science Fund, China (No.0832257)the Research Funds of Education Bureau of Guangxi Province, China (No.200708LX333)
文摘Barium strontium titanate (Ba 0.5 Sr 0.5 TiO 3 , BST)/silicon nanoporous pillar array (Si-NPA) thin films were prepared by a spin-coating/annealing technique based on Si-NPA with micro/nano-structure. Both the isomer conversion of acetylacetone and the network structure combined by enol and Ti-alkoxide facilitate the formation of the BST sol and the subsequent crystallization. Before the perovskite BST begins to form, the intermediate phase (Ba,Sr)Ti 2 O 5 CO 3 is found. The boundary between BST and Si-NPA is of clarity and little interface diffusion, disclosing that Si-NPA is an ideal template substrate in the preparation of multifunctional composite films.
