In this work, the influence of the sintering temperature on the physical properties of (Pb0.8La0.2)(Ti0.9Ni0.1)O3 (PLT-Ni) ceramics is reported. The experimental data revealed that the energy band gap of PLT-Ni ceramics could be tailored from approximately 2.7 to 2.0 eV by changing the sintering temperature from 1100°C to 1250°C. It is demonstrated that the simple substitution of Ti4+ by Ni2+ cations is effective to decrease the intrinsic band gap while increasing the tetragonality factor and the spontaneous polarization. However, the additional red-shift observed in the absorption edge of the PLT-Ni with increasing the sintering temperature was associated with a continuous increase in the oxygen vacancies () amount. It is believed that the impact of the creation of these thermally induced is manifold. The presence of and Ni2+ ions generate the Ni2+- defect-pairs that promoted both a decrease in the intrinsic band gap and an additional increase of the tetragonality factor, consequently, increasing the spontaneous polarization. The creation of Ni2+- defects also changed the local symmetry of Ni2+ ions from octahedral to a square pyramid, thus lifting the degeneracy of the Ni2+ 3d orbitals. With the increase in the sintering temperature, lower-energy absorbing intraband states were also formed due to an excess of , being responsible for an add-on shoulder in the absorption edge, extending the light absorption curve to longer wavelengths and leading to an additional absorption in “all investigated” spectrum as well. 相似文献
Five candidate pheromone components were identified by analyzing pheromone gland extracts by gas chromatography (GC), coupled GC-electroantennographic detection (EAD), and coupled GC-mass spectrometry (MS): (E)-11-hexadecenol(E11–16 : OH), (Z)-11-hexadecenol (Z11–16 : OH),(E)-11-hexadecenal, (E)-11-hexadecenyl acetate, and (Z)-3,(Z)-6,(Z)-9-tricosatriene (Z3,Z6,Z9–23 : Hy). In electroantennogram (EAG) recordings, synthetic E11–16 : OH elicited stronger antennal responses at low doses than other candidate pheromone components. Field tests demonstrated that synthetic E11–16 : OH as a trap bait was effective in attracting males, whereas addition of Z11–16 : OH inhibited the males' response. Z3,Z6,Z9–23 : Hy strongly enhanced attractiveness of E11–16 : OH, but was not attractive by itself. A pheromone blend with synergistic behavioral activity of an alcohol (E11–16 : OH) and hydrocarbon (Z3,Z6,Z9–23 : Hy) component is most unusual in the Lepidoptera. The synthetic two-component pheromone is approximately 60 times more attractive than the female-produced blend and might facilitate the control of this pest. 相似文献
Three new dihydro--agarofuran sesquiterpenes from two species ofMaytenus were isolated and their structures were elucidated by means of1H and13C NMR studies. The differences and similarities noted in the chemical content of the dihydro--agarofuran sesquiterpenes from the fourMaytenus species from Chile are in line with the taxonomic characterization of these species; their geographical distribution is also given. 相似文献
The properties are described of low-ammonia latex concentrates produced by gamma-ray irradiation (0.5–2.0 Mrad dose) in the presence of carbon tetrachloride or chloroform as sensitizer. Dipping trials with irradiated concentrates and irradiated field latex, for the preparation of condoms and medical gloves, gave products with high ultimate elongation, low modulus, and high permanent set. A change from straight dipping and a heat treatment after drying resulted in improved physical properties. A notable feature of products prepared from these materials is their purity, i.e., low content of rubber chemicals. An economic disadvantage, at the present time, is the high initial cost of the irradiation equipment. 相似文献
Thermotropic polyesters prepared from series of 4,4-dihydroxy-,w-diphenoxy alkanes and 4,4-dichloroformyl-,w-diphenoxy alkanes are well known. The substitution of a methylenic spacer by an oxyethylenic spacer in the main chain of these polyesters drastically modifies their physical properties, particularly the mesogenic transition temperatures, as can be observed by DSC and thermooptical analysis. The thermal stability and the polymer solubility in common organic solvents of these polymers did not show a significant change. The physical properties of the two thermotropic polyesters prepared in diphenyl ether were evaluated. 相似文献
High molecular weight poly(α-methyl β,l-malate) (Mn ∼ 25,000, PD ∼ 1.7) was prepared from microbial poly(β,l-malic acid) (Mn ∼ 29,000, PD ∼ 1.3) by methylation with diazomethane in dry acetone without substantial cleavage of the polyester main chain. The thermal properties of this poly(malate) were assessed and its crystal structure was preliminary examined. Two crystal forms were identified by X-ray diffraction, their occurrence being dependent on crystallization conditions. The kinetics of nonisothermal and isothermal crystallizations from the melt were studied and modelled using the Avrami approach. Results were compared to those recently reported by us for low molecular weight poly(α-methyl β,l-malate) (Mn ∼ 3000, PD ∼ 1.3). 相似文献
Modification of chitosan by grafting of vinyl butyrate was carried out in homogeneous phase using potassium persulfate as
redox initator and 1.5% acetic acid as solvent. The percent grafting and grafting efficiency were analysed and the high grafting
efficiency up to 94% was observed. The effects of reaction variables such as monomer concentration, initiator concentration,
temperature and reaction time were investigated. It was observed that the solubility of chitosan was markedly reduced after
grafting with vinyl butyrate. The grafted product is insoluble in common organic solvents as well in dilute organic and inorganic
acids. Characterization of the graft copolymers were carried out by using Fourier Transform Infrared Spectroscopy (FTIR),
Differential Scanning Calorimetry (DSC) and Scanning Electron Microscopy (SEM) technics. Characteristic signal of carbonyl
group was observed at 1,731 cm−1 which belongs to the poly vinyl butyrate segments in the graft copolymer. The melting transition of the chitosan main chain
in the copolymer shifted to 124°C from its original value 101°C. In addition to these, we have also studied topology of the
graft copolymer and the SEM micrograph showed continuous homogenous matrix which means there is no phase separation. 相似文献
The deposition-precipitation method was used to prepare gold catalysts based on different supports. Their catalytic activities for combustion of carbon monoxide (CO) and formaldehyde (HCHO) were investigated. All these catalysts showed good activity for the two reactions and the Au/CeO2-a catalyst exhibited the highest activity for the two reactions. Furthermore, catalysts derived from the as-precipitate hydroxides exhibited higher activity than that from corresponding oxide supports. The BET, XRD, TEM and XPS were carried out. The results indicated that the gold dispersed more homogeneous on the as-precipitate hydroxide supports than that on the corresponding oxide supports. 相似文献
Summary: The dicationic [(dppp)Pd(NCCH3)2](BF4)2 catalyst (dppp = 1,3‐bis(diphenylphosphino)propane) was applied in a liquid monomer, two phase process for the CO/propene copolymerization reaction. For the first time it was possible to synthesize propene/CO copolymers with an activity up to 7 500 g/(mol · h) and molecular weights of 500 000 g/mol. Activities up to 40 000 g/(mol · h) could be obtained with the use of the unsymmetric catalyst [(CF3‐dppp)Pd(NCCH3)](BF4)2 (CF3‐dppp = 1‐diphenylphosphino‐3‐bis[3,5‐di(trifluormethyl)phenyl]phosphinopropane) in homogeneous liquid propene solution.