AlPO_4-5负载溴化铝催化酮的Baeyer-Villiger氧化反应

以异丙醇铝为铝源,正磷酸为磷源,三乙胺作模板剂,采用水热反应合成了AlPO4-5分子筛。应用不同浓度氢溴酸对AlPO4-5分子筛进行化学剪裁,制备AlPO4-5-AlBr3催化剂。FESEM、XRD、N2吸附-脱附等表征结果表明,合成的AlPO4-5是规整的微孔六方棱柱,化学剪裁制备的担载型催化剂AlPO4-5-AlBr3依然保持规整的六方棱柱。催化氧化实验表明,质量分数30%双氧水作为氧化剂,在乙酸乙酯溶剂中,催化剂AlPO4-5-AlBr3对部分环酮具有较好的催化活性。     

Structural study of the 0.4-nm single-walled carbon nanotubes aligned in channels of AlPO4-5 crystal

A detailed synthesis process of ultra-small single-walled carbon nanotubes (SWNTs) aligned in the channels of AlPO₄-5 zeolite single crystals is reported. The structure of such ultra-small SWNTs was analyzed by means of transmission electron microscopy (TEM) and polarized Raman scattering. TEM images showed that the diameter of the SWNTs is as small as 0.4 nm, which is the size of three possible structures: the zigzag (5,0), armchair (3,3) and chiral (4,2). The polarization dependence of the Raman lines indicates that the structures of the nanotubes are dominated by the zigzag (5,0) form. Line-shape analysis of the tangential A_1g Raman mode shows that the SWNTs are metallic with a finite electronic density-of-state near the Fermi energy level, which is in agreement with the band structural calculation using local-density function approximation (LDA) as well as the electric transport measurement.     

On stability and performance of highly c-oriented columnar AlPO4-5 and CoAPO-5 membranes

Continuous films comprised of highly c-oriented aluminophosphate AlPO₄-5 or cobalt-substituted AlPO₄-5 (CoAPO-5) were grown on porous supports and subjected to heat treatment in order to investigate the potential for membrane applications. A study in the early stages of in-plane crystalline intergrowth revealed a potential mechanism for flake-like crystal formation between the original oriented columnar crystals. Variations in metal substitution (AlPO₄-5, CoAPO-5), support (glass, silicon, porous alumina), and calcination method (conventional, rapid thermal processing) were chosen to examine the conditions by which structural integrity was compromised following secondary (or tertiary) growth, resulting in reduced membrane functionality. Through the use of rapid thermal processing, the structure debilitation could be partially avoided. The membrane quality was inspected through pervaporation measurements consisting of a liquid hydrocarbon feed of n-heptane and 1,3,5-triisopropylbenzene. By investigating the effect of template removal on the oriented, columnar crystalline structure, useful insight is provided into the potential for the membranes to participate in applications such as molecular separations, catalysis, or host-guest assemblies.     

Microstructure of selectively heated (hot spot) region in Fe3O4 powder compacts by microwave irradiation

An Fe₃O₄ powder compact was irradiated with a 2.45 GHz microwave single-mode applicator at the magnetic field maximum position. Selectively heated regions (hot spot region) having several hundred micrometers to millimeter scale were formed. They exhibited metallic color. The SEM/EDX observations showed no appreciable difference in the compositions between the hot spot regions and the matrix. However, micro-XRD revealed that the hot spot region had a larger fraction of FeO than the matrix did, although the major consisting phase was Fe₃O₄ with a little Fe₂O₃. TEM observations indicated that the observed hot spot regions comprise these oxide phases separated in nano-sized grains, which agrees with our previous report. The larger fraction of FeO phase and flat surface might be related with the metallic color of the hot spot region. Their formation mechanisms and phase constitution were discussed.     

In situ growth of AlPO4-5 molecular sieve on stainless steel support

A continuous coating on stainless steel mesh with AFI-type molecular sieve was achieved by a simple one-step in situ synthesis. AlPO₄-5 crystals have been grown directly on the surface of the substrate. Influences of composition of the staring reaction solution and crystallization temperature on the morphology and the orientation of crystals on the support were investigated. It was shown that the crystals in the coating grew along their one-dimensional channel perpendicular to the substrate when using the synthesis solution with the molar ratio of Al₂O₃:1.3P₂O₅:1.2TrEA:200H₂O. Stainless steel slice was also used as the substrate to study the growth of molecular sieve AlPO₄-5 film at similar synthesis conditions. A competitive growth model was implied to explain the formation of c-axis oriented film based on the observations. The supported coatings were characterized by scanning electron microscopy and X-ray diffractions.     

微波辐射下CaSO4生成反应过程中的热点特性

在微波辐射化学反应过程中,常常会因为存在热点而导致爆炸或反应物烧毁等现象发生。本文以微波辐射下的硫酸钙生成反应为例,利用有限元方法求解Maxwell方程组、流体力学方程以及热传导方程,研究了微波辐射反应过程中热点的变化情况,并用实验验证了计算结果的正确性。研究结果表明：在加热过程中,随反应的进行,热点的位置是在不断变化的,且热点常出现在物质分相界面附近。     

Hydrodesulfurization and hydrodearomatization activities of catalyst containing ETS-10 and AlPO4-5 on Daqing FCC diesel

A Ni–W loaded ETS-10/AlPO₄-5/Al₂O₃ composite support catalyst was optimized and used in hydrodesulfurization (HDS) and hydrodearomatization (HDA) of Daqing FCC diesel feedstock. The result indicated that ETS-10 and AlPO₄-5 showed positive synergism effect. The effects of operating conditions on its catalytic performance were investigated by using a 100 mL hydrotreating test unit. The catalyst showed a remarkable HDS conversion of 99.9% and a HDA conversion of 73.2%. A clean diesel product with ultra-low sulfur content (<1.0 μg/g) and very low polycyclic aromatic content (<2.0 wt.%) was obtained.     

Preparation and characterization of nano-sized LiFePO4 by low heating solid-state coordination method and microwave heating

The precursors of LiFePO₄ were prepared by low heating solid-state coordination method using lithium acetate, ammonium dihydric phosphate, ferrous oxalate and citric acid as raw materials. Olivine phase LiFePO₄ as a cathode material for lithium-ion batteries was successfully synthesized by microwave heating in a few minutes. X-ray diffraction (XRD) and transmission electron microscope (TEM) were used to characterize its structure and morphology. Cyclic voltammetry (CV) and charge-discharge cycling performance were used to characterize its electrochemical properties. The results showed that the grain size of the optimal sample was about 40-50 nm, and the as-prepared particles were homogeneous. The nano-sized LiFePO₄ obtained has a high electrochemical capacity (125 mAh g⁻¹) and stable cycle ability.     

Comparison of AlPO4- and Co3(PO4)2-coated LiNi0.8Co0.2O2 cathode materials for Li-ion battery

Electrochemical and thermal properties of Co₃(PO₄)₂- and AlPO₄-coated LiNi_0.8Co_0.2O₂ cathode materials were compared. AlPO₄-coated LiNi_0.8Co_0.2O₂ cathodes exhibited an original specific capacity of 170.8 mAh g⁻¹ and had a capacity retention (89.1% of its initial capacity) between 4.35 and 3.0 V after 60 cycles at 150 mA g⁻¹. Co₃(PO₄)₂-coated LiNi_0.8Co_0.2O₂ cathodes exhibited an original specific capacity of 177.6 mAh g⁻¹ and excellent capacity retention (91.8% of its initial capacity), which was attributed to a lithium-reactive Co₃(PO₄)₂ coating. The Co₃(PO₄)₂ coating material could react with LiOH and Li₂CO₃ impurities during annealing to form an olivine Li_xCoPO₄ phase on the bulk surface, which minimized any side reactions with electrolytes and the dissolution of Ni⁴⁺ ions compared to the AlPO₄-coated cathode. Differential scanning calorimetry results showed Co₃(PO₄)₂-coated LiNi_0.8Co_0.2O₂ cathode material had a much improved onset temperature of the oxygen evolution of about 218 °C, and a much lower amount of exothermic-heat release compared to the AlPO₄-coated sample.     

Crystal structures and microwave dielectric properties of low-firing Ca5Zn4-xMgxV6O24 ceramics

Ca₅Zn_4-xMg_xV₆O₂₄ (x?=?0–3) microwave dielectric ceramics with low sintering temperature were synthesized via the conventional solid-state reaction. Effects of the substitution of Mg²⁺ for Zn²⁺ on crystal structures and microwave dielectric properties were investigated. XRD and Rietveld refinement showed the solid solution single phase formed when 0?≤?x?≤?2, but a few ZnO was observed when x?=?3. Meanwhile, the lattice parameters were found to decrease monotonously with Mg content increasing. The vibration modes of Raman were confirmed and the relationship with microwave dielectric properties was analyzed. Appropriate substitution of Mg²⁺ improved the packing fraction, the cation ordering degree, and the Y-site bond valence, contributing to high Q×f and low | τ_f |. However, the ε_r reduced with the increasing content of Mg²⁺ due to the decrease of ion polarizability. Finally, the best microwave dielectric properties were achieved at x?=?2 with ε_r =?11.0, Q?×?f?=?66,365?GHz (at 10.0?GHz), and τ_f =??80.4?ppm/°C.     

Catalytic effect of metal cations on the formation of carbon nanotubes inside the channels of AlPO4-5 crystal

Single-walled 0.4 nm carbon nanotubes (SWNTs) were fabricated using various metal cation substituted AlPO₄-5 (MeAPO-5) molecular sieves as the template. The catalytic behavior varies with different metal incorporation. The incorporation of metal cations (Mn, Mg, Co) and Si gives rise to the formation of negatively charged frameworks and Brønsted acid sites. These frameworks thus play an important catalytic role in the pyrolysis and conversion of the organic molecules to SWNTs within the crystal channels. It is shown that the MeAPO-5 single crystals have a higher density of SWNTs than those crystals without the metal cations. The experimental results agree with the predictions of first-principles calculations, which show the metal-incorporated frameworks to be favorable for the SWNTs formation.     

Crystal structure and electrochemical performance of Li3V2(PO4)3 synthesized by optimized microwave solid-state synthesis route

To investigate the crystal structure and electrochemical performance of samples synthesized under different microwave solid-state synthesis condition, a series of Li₃V₂(PO₄)₃ samples has been synthesized at five different temperatures for 3-5 min and at 750 °C for various time. The as-synthesized Li₃V₂(PO₄)₃ samples are characterized and studied by ICP-AES analysis, X-ray diffraction (XRD), Rietveld analysis, scanning and transmission electron microcopy (SEM and TEM). At relatively lower temperature (650 °C) and very short reaction time (3 min), pure phase of Li₃V₂(PO₄)₃ could be synthesized in microwave irradiation field. The crystal structure and Li atomic fractional coordinate present a significant deviation upon the change of microwave irradiation temperature and time. Relatively, the diffusion ability of lithium cations and the electrochemical performance are affected. Under the proper reaction temperature and time, the carbon-free samples MW750C5m and MW850C3m show the best specific discharge capacity 126.4 and 132 mAh g⁻¹ at the voltage range of 3.0-4.3 V, near the reversible cycling of two lithium ions per Li₃V₂(PO₄)₃ formula unit (133 mAh g⁻¹). At the voltage range of 3-4.8 V, the sample MW750C5m presents the best initial specific charge capacity of 197 mAh g⁻¹, equivalent to the reversible cycling of three lithium ions per Li₃V₂(PO₄)₃ formula unit (197 mAh g⁻¹). The initial discharge capacity, the samples MW750C5m and MW850C3m present high specific discharge capacity 183.4 and 175.7 mAh g⁻¹, respectively. The relationship among microwave irradiation condition, crystal structure, lithium atomic fractional coordinates and the electrochemical performance have been discussed in detail.     

Catalytic pyrolysis of Athabasca bitumen in H2 atmosphere using microwave irradiation

Microwave-assisted catalytic pyrolysis was carried out for upgrading of Athabasca bitumen. The bitumen can be heated to the desired target temperature (430 °C) for pyrolysis with silicon carbide (SiC), a heating element, in approximately 10 min under microwave irradiation. However, the pyrolysis with SiC only resulted in heavy and viscous liquid product having an API gravity of 17.14°. Addition of Nickel and Molybdenum nanoparticles as catalysts enhanced the pyrolysis performance in terms of liquid yield and quality. In the pyrolysis with Mo nanoparticles, the yield and the API gravity of the liquid product were 72.0 wt% and 20.98°, respectively. However, the separate existence of nanoparticles and SiC in the reactor and the recovery problem of nanoparticles, might limit their application in microwave-assisted pyrolysis. In order to prepare a composite with microwave susceptibility and catalytic activity in one body, transition metals were loaded on alumina coated SiC. When it is compared to the direct application of metal nanoparticles to the pyrolysis of bitumen, the NiMo/Al₂O₃/SiC catalyst showed enhanced catalytic performance. The API gravity and sulfur contents of the liquid products from the pyrolysis with NiMo/Al₂O₃/SiC were 22.42° and 2.84 wt%, respectively.     

Crystal structure,microwave dielectric properties and low temperature sintering of (Al0.5Nb0.5)4+ co-substitution for Ti4+ of LiNb0.6Ti0.5O3 ceramics

The phase composition, microstructure, microwave dielectric properties of (Al_0.5Nb_0.5)⁴⁺ co-substitution for Ti site in LiNb_0.6Ti_0.5O₃ ceramics and the low temperature sintering behaviors of Li₂O-B₂O₃-SiO₂ (LBS) glass were systematically discussed. XRD patterns and EDS analysis result confirmed that single phase of Li_1.075Nb_0.625Ti_0.45O₃ solid solution was formed in all component. The increase of dielectric constant (ε_r) is ascribed to the improvement of bulk density. The restricted growth of grain has a negative influence on quality factor (Q×f) value. The τ_f value could be continuously shifted to near zero as the doping content increases. Great microwave dielectric properties were obtained in LiNb_0.6Ti_(0.5-x)(Al_0.5Nb_0.5)_xO₃ ceramics (x?=?0.10) when sintered at 1100?℃ for 2?h: ε_r =?70.34, Q×f =?5144?GHz, τ_f =?4.8?ppm/℃. The sintering aid, LBS glass, can effectively reduce the temperature and remain satisfied microwave performance. Excellent microwave dielectric properties for x?=?0.10 were obtained with 1.0?wt% glass: ε_r =?70.16, Q×f =?4153?GHz (at 4?GHz), τ_f =?-0.65?ppm/℃ when sintered at 925?℃ for 2?h.     

Fabrication and characterization of monodispersed Mn0.8Ni0.2Co2O4 mesoporous microspheres for supercapacitor application

The monodispersed Ni doped MnCo₂O₄ mesoporous microspheres were synthesized through a simple ammonium bicarbonate-assisted solvothermal route. The spinel-type crystal structure with a lattice parameter of 8.199?Å for Mn_0.8Ni_0.2Co₂O₄ composition was obtained by using X-ray diffraction analysis. The Brunauer?Emmett?Teller (BET) specific surface area of the sample was found to be 75.78?m² g^?1 with an average pore diameter of 9.88?nm. Electron microscopy studies revealed that the stable mesoporous microspheres are constituted by well-connected aggregates of nanoparticles. The influence of Ni doping on the pseudo-capacitance of MnCo₂O₄ electrode was investigated by means of cyclic voltammetry in 6?M KOH electrolyte. We found that the spinel-type Mn_0.8Ni_0.2Co₂O₄ mesoporous microspheres exhibit specific capacitances of 1822 F g^?1 at a scan rate of 5?mV/s. Furthermore, the electrochemical impedance spectroscopy analysis revealed the low resistance and good electrochemical stability of the sample.     

Structural evolution and microwave dielectric properties in Sr2(Ti1-xSnx)O4 ceramics

The structure and microwave dielectric properties of Sr₂(Ti_1-xSn_x)O₄ ceramics were determined in the entire composition range of x?=?0–1.0. X-ray diffraction patterns and Raman spectra indicated a composition-induced onset of octahedral tilting at x?=?0.75, and the crystal structure transformed from tetragonal (I4/mmm) to orthorhombic (Pccn). An obvious change of grain morphology was observed in the phase transformation region as well. The variations of the microwave dielectric properties with composition were systematically investigated and the effect of octahedral tilting on the evolution of τ_f value was emphasized. Moreover, the relationship between τ_ε and tolerance factor of the present ceramics was revealed and compared with the empirical rule in perovskite structure. The role of tolerance factor in designing the materials with required performance was highlighted.     

Structural and photocatalytic degradation characteristics of hydrothermally treated mesoporous TiO2

Mesoporous TiO₂ photocatalysts have been synthesized using polyethylene glycol (PEG) as a template direction agent in diluted acetic acid aqueous solution. This medium slows down the hydrolysis reaction of titanium sources due to the hydrolytic retardant and the strong chelating effects of acetic acid. A hydrothermal treatment process was introduced to better control the resultant mesoporous structures. The effects of PEG molecular weight and thermal treatment temperature on the resultant structure and photoactivity were investigated. Morphological, structural and phase compositional properties of the resultant photocatalysts were systematically characterized using transmission electron microscopy, X-ray diffraction and nitrogen adsorption/desorption analysis. The mesoporous structure with diameters between 13.3 and 17.0 nm and mean porous sizes that ranged from 9.6 to 13.3 nm were obtained when the molecular weight of PEG were varied from 200 to 20,000. The mesoporous diameters were changed significantly from 9.8 to 18.4 nm with mean porous sizes slightly increasing from 8.0 to 10.0 nm when the calcination temperature was varied from 350 to 550 °C. The activities of the resultant TiO₂ photocatalysts were evaluated using 2,4,6-tribrominated phenol as a testing compound that represents a class of toxic brominated flame retardants. The experimental results revealed that the photocatalytic activity depends on the phase and on the structural characteristics of the resultant photocatalysts.     

Synthesis and structure of AlPO4-9: An unacquainted member in the family of microporous aluminophosphates

In the family of microporous aluminophosphate, AlPO₄-9 is one of the members reported first in 1982. However, its structure and characteristics have not been known up to now, and this makes it a special member. In the present work, AlPO₄-9 has been synthesized using piperazine as the structure-directing agent and the mixture of H₂O and EG as the solvent. Structure refinement from single crystal X-ray diffraction data shows that AlPO₄-9 is a material with the composition of C₂H₇Al_5.50NO₂₅P₆. It crystallizes in the monoclinic space group C2/c (No: 15), with a = 24.230(5) Å, b = 14.026(5) Å and c = 16.197(3) Å, β = 119.87(4)°, V = 4773(2) Å³, Z = 8. The open-framework of AlPO₄-9 is built of alternating corner-sharing PO₄ tetrahedra and AlO₄ tetrahedra (AlO₆ octahedra) to construct a curved one-dimensional 8-ring channel system running along [1 0 1]. Meanwhile, the strict alternative of PO₄ tetrahedra and AlO₄ tetrahedra (AlO₆ octahedra) results in a negative framework in AlPO₄-9. Thermal stability has been determined on a thermal analyzer and by calcination. It reveals that AlPO₄-9 framework is thermally stable and has a potential to be a catalytic material.     

Effects of (Cr0.5Ta0.5)4+ on structure and microwave dielectric properties of Ca0.61Nd0.26TiO3 ceramics

The Ca_0.61Nd_0.26Ti_1-x(Cr_0.5Ta_0.5)_xO₃ (CNT-CTx) ceramics with orthorhombic perovskite structure were prepared using the conventional solid-state method. The X-ray diffraction (XRD), Raman spectra and X-ray photoelectron spectra (XPS) were employed to investigate the correlations between crystal structure and microwave dielectric properties of CNT-CTx ceramics. The XRD results showed that all CNT-CTx samples were crystallized into the orthorhombic perovskite structure. The SEM micrographs indicated that the average grain size of samples depended on the sintering temperature. As (Cr_0.5Ta_0.5)⁴⁺ concentration increased, there was a significant decrease in the average grain size of samples. The short range order (SRO) structure and structural distortion of oxygen octahedra proved to exist in CNT-CTx crystals according to the analysis of Raman spectra results. The microwave dielectric properties highly depended on the full width at half maximum (FWHM) of Raman spectra, oxygen octahedra distortion, reduction of Ti⁴⁺ to Ti³⁺ and bond valence. At last, the CNT-CT0.05 ceramic sintered at 1420?°C for 4?h exhibited the good and stable comprehensive microwave dielectric properties: relative permittivity of 96.5, quality factor of 14,360?GHz, and temperature coefficient of resonant frequency of +153.3?ppm/°C.     

Synthesis and characterization of mesoporous Ta2O5–TiO2 photocatalysts for water splitting

Two series of Ta₂O₅–TiO₂ photocatalysts (Ta:Ti = 4:1, 1:1 and 1:4) were prepared by sol–gel technique applying triblock copolymer of Pluronic P123 and were tested in platinized form (0.3 wt.%) in photodecomposition of water under ultraviolet and visible light (λ > 300 nm). It was found the mesoporous character of tantalum containing catalysts with relatively high surface area (100–130 m² g⁻¹) of these samples. However, higher concentration of TiO₂ in mixed oxides leads to the destruction of mesoporous character of synthesized photocatalysts. All samples were characterized with thermogravimetry, XRD, N₂ physisorption, DR-UV–vis and FTIR spectroscopy. The mixed oxides of Ta₂O₅–TiO₂ system showed much lower band-gap than pure Ta₂O₅ and relatively high activity in platinized state in photocatalytic hydrogen generation under visible. Doping of pure oxides and mixed systems with sulfur resulted in lowering of the band-gap values below 3 eV and much better activity in H₂ evolution reaction. Non-platinized photocatalysts showed activity in liquid phase cyclohexene photooxidation at 305 K.