P, N, and Mo ternary co-doped nano TiO2 photocatalysts ((P, N, Mo)-TiO2) were prepared by a single step sol–gel method, which show much enhanced photocatalytic activities over Mo-TiO2, (P, N)-TiO2, un-doped TiO2 and Degussa P25 under visible light irradiation. The degradation rate of 0.72Mo–P-TiO2 is as high as 65.3%, which is about 6.7 times of that of Degussa P25. Possible reasons for the improvement of photocatalytic
activities were analyzed. 相似文献
Flower power : Various mesoporous Co3O4 architectural structures (see figure) have been successfully prepared through a facile binary‐solution route and sequential thermal decomposition at atmospheric pressure. The electrochemical experiments showed that the specific capacitance of Co3O4 nanosheets was higher than that of Co3O4 microspheres in a KOH electrolyte.
A new method for the simultaneous determination of fluorine and iodine in urine by ion chromatography(IC) with electrochemical pretreatment has been developed.The pretreatment was performed in a novel electrochemical oxidation-neutralization device(EOND),in which iodide of the sample was oxidized to iodate and the alkaline digestion sample solution was neutralized.Under the optimized conditions,the limits of detection(LOD,S/N = 3) were 2.5μg/L for fluoride and 20μg/L for iodate,respectively.The recoverie... 相似文献
Liquid chromatography–electrospray ionization mass spectrometry has been used for rapid, selective, and sensitive quantitative analysis of mitiglinide in human plasma. Sample pretreatment involved solid-phase extraction from plasma with gliclazide as internal standard. Separation was performed on a C18 column (150 × 2.0 mm) with 71:29 (v/v) acetonitrile–water (containing 0.1% formic acid and 0.2 mmol L?1 ammonium acetate) as mobile phase at a flow rate of 0.2 mL min?1. The method was validated then successfully applied to a clinical bioequivalence study of mitiglinide in 20 healthy volunteers after oral administration. 相似文献
Nanocrystals are fundamental to modern science and technology. Mastery over the shape of a nanocrystal enables control of its properties and enhancement of its usefulness for a given application. Our aim is to present a comprehensive review of current research activities that center on the shape‐controlled synthesis of metal nanocrystals. We begin with a brief introduction to nucleation and growth within the context of metal nanocrystal synthesis, followed by a discussion of the possible shapes that a metal nanocrystal might take under different conditions. We then focus on a variety of experimental parameters that have been explored to manipulate the nucleation and growth of metal nanocrystals in solution‐phase syntheses in an effort to generate specific shapes. We then elaborate on these approaches by selecting examples in which there is already reasonable understanding for the observed shape control or at least the protocols have proven to be reproducible and controllable. Finally, we highlight a number of applications that have been enabled and/or enhanced by the shape‐controlled synthesis of metal nanocrystals. We conclude this article with personal perspectives on the directions toward which future research in this field might take. 相似文献
A modified nano-calcium carbonate (R-CCR) was prepared by coating a layer of unsaturated hydroxylfatty acid on the surface
of CCR powders using a solid state method; the latter were commercial nano-CaCO3 modified with stearic acid. FTIR studies indicate that the modifier is combined on the surface of CaCO3. PP/EPDM/nano-CaCO3 ternary composites were prepared by a melt-mixing method. SEM and TEM were utilized to examine the morphology of the composites.
The tensile fractured surface of PP/EPDM/R-CCR showed a fibroid morphology and large-scale yield deformation. The impact fractured
surface showed that the amount of cavities in the PP/EPDM/R-CCR system was increased, however their size diminished obviously.
R-CCR particles were dispersed uniformly in the PP matrix, and their compatibility was distinctly improved as compared to
CCR when the amount of R-CCR was 15 h−1. The tensile strength remained nearly constant (reduced from 27.6 MPa to 27.5 MPa), while the impact strength increased from
9.6 kJ/m2 to 15.4 kJ/m2 as CCR was replaced by R-CCR. Meanwhile, the bending strength and bending modulus also increased correspondingly. Furthermore,
the impact strength of PP/EPDM/R-CCR was maintained at a high level (15.4 kJ/m2), which was more than the sum of that of PP/EPDM and PP/R-CCR (6.6 kJ/m2 and 6.1 kJ/m2 respectively). This indicates that the R-CCR and EPDM have a significant synergistic toughening effect on PP while maintaining
the strength and modulus of virgin PP. Both the storage modulus G′ and loss modulus G″ of PP/EPDM and PP/EPDM/R-CCR composites increase with increasing frequency, but the values of G′ and G″ of the tertiary composite are relatively higher than those of the binary system. The loss factor and viscosity decrease with
increasing frequency, but there is little difference between tertiary and binary composites. The apparent viscosity η of the tertiary system containing R-CCR is lower than that of the tertiary system containing CCR and virgin PP. The viscosity
of the composites sig-nificantly decreases with increasing shear rate. The mea-sured mechanical properties of the composites
indicate that replacing CCR with R-CCR for binary composites could simultaneously enhance the toughness and strength of PP.
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Translated from Acta Polymerica Sinica, 2008, 4 (in Chinese) 相似文献
In the chiral polymeric title compound, poly[aqua(4,4′‐bipyridine)[μ3‐S‐carboxylatomethyl‐N‐(p‐tosyl)‐l ‐cysteinato]manganese(II)], [Mn(C12H13NO6S2)(C10H8N2)(H2O)]n, the MnII ion is coordinated in a distorted octahedral geometry by one water molecule, three carboxylate O atoms from three S‐carboxyatomethyl‐N‐(p‐tosyl)‐l ‐cysteinate (Ts‐cmc) ligands and two N atoms from two 4,4′‐bipyridine molecules. Each Ts‐cmc ligand behaves as a chiral μ3‐linker connecting three MnII ions. The two‐dimensional frameworks thus formed are further connected by 4,4′‐bipyridine ligands into a three‐dimensional homochiral metal–organic framework. This is a rare case of a homochiral metal–organic framework with a flexible chiral ligand as linker, and this result demonstrates the important role of noncovalent interactions in stabilizing such assemblies. 相似文献
When applied to the classical dynamical equations, generally, conventional time-stepping methods cannot conserve the total energy exactly, but up to their algebraic order. To obtain an energy-conserving method, we add an energy calibrated parameter to some conventional ones. The periodic stability and phase-lag property of this type of energy-conserving methods are investigated in this note. Some numerical results are reported to illustrate our conclusions. 相似文献