A series of BiOX(X=Cl,Br) were prepared by simple hydrolysis and then calcined at various temperatures and they were characterized by XRD,Raman,SEM,DSC-TGA,BET and UV-Vis.The photocatalytic activity was evaluated by p...A series of BiOX(X=Cl,Br) were prepared by simple hydrolysis and then calcined at various temperatures and they were characterized by XRD,Raman,SEM,DSC-TGA,BET and UV-Vis.The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange(MO) solution under simulated solar light irradiation.The results show that the phase structure,crystallite size,morphology,specific surface area,porous structure,and the absorption band-edges are related to the calcination temperature.For BiOBr,it has completely transformed to Bi24O31Br10 at 600℃ and begins to transform to Bi2 O3 at 800℃.As for BiOCl,it begins to transform to Bi24O31Cl10 at 600℃ and completely transforms to Bi24O31Cl10 at 800℃.Finally,the photocatalytic activity of BiOCl decreases with the temperature increasing owing to decrease of the specific surface areas and pore size,while the photocatalytic activity of BiOBr increases in the first stage and then decreases,which is related to good crystallization and three-dimensional structure.展开更多
This paper represents the interaction of well characterized Lewis base [（Pyr）nCuX]4O2, n = 1 or 2, X = Cl, Br or I, Pyr = pyrrolidine with CO2 as a Lewis acid to produce new series of oxidative coupling and catechol...This paper represents the interaction of well characterized Lewis base [（Pyr）nCuX]4O2, n = 1 or 2, X = Cl, Br or I, Pyr = pyrrolidine with CO2 as a Lewis acid to produce new series of oxidative coupling and catechol oxidase initiators [（Pyr）nCuX]4（CO3）2. These carbonato derivatives are isolated as stable solids. They are easily soluble in aprotic solvents as CH2Cl2 or PhNO2. Cryoscopic measurements support tetranuclear core structure for all of them. Infrared spectra show differences from their oxo analogous in the carbonato domains but those differences did not distinguish between tridentate bridging carbonato and bidentate one. Rate of oxidation of 2,6-dimethylphenol （DMP） by [（Pyr）CuCl]4（CO3）2, supports coordination number six for Cu（Ⅱ） centers in [（Pyr）CuCl]4（CO3）2. In order to fulfill coordination number six, for n = 1, carbonate will act as tridentate while for n = 2, it will act as bidentate, as shown in Scheme 4. Near infrared spectra indicate a [（3 halo） Cu（Ⅱ） charge transfer] for [（Pyr）nCuX]4（CO3）2, n = 1 or 2, X = Cl or Br. Low molecular absorptivities of the maxima at 825 nm and 730 nm for [（Pyr）nCuI]4（CO3）2, n = 1 or 2 with a minimum of high molecular absorptivities at 600 nm, comparing to X= CI or Br analogous, support a step structure for [（Pyr）,Cul]4（CO3）2, as shown in Scheme 5. Cyclic voltammograms for [（Pyr）nCuX]4（CO3）2; n = 1 or 2, X = CI or Br, are irreversible in characters.展开更多
基金Projects(21676178,21506144,21706179)supported by the National Natural Science Foundation of ChinaProject(2019L0138)supported by the Science and Technology Innovation Program of Higher Education Institutions in Shanxi Province,ChinaProject(201901D211100)supported by the Natural Science Foundation of Shanxi Province for Young Scientists,China
文摘A series of BiOX(X=Cl,Br) were prepared by simple hydrolysis and then calcined at various temperatures and they were characterized by XRD,Raman,SEM,DSC-TGA,BET and UV-Vis.The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange(MO) solution under simulated solar light irradiation.The results show that the phase structure,crystallite size,morphology,specific surface area,porous structure,and the absorption band-edges are related to the calcination temperature.For BiOBr,it has completely transformed to Bi24O31Br10 at 600℃ and begins to transform to Bi2 O3 at 800℃.As for BiOCl,it begins to transform to Bi24O31Cl10 at 600℃ and completely transforms to Bi24O31Cl10 at 800℃.Finally,the photocatalytic activity of BiOCl decreases with the temperature increasing owing to decrease of the specific surface areas and pore size,while the photocatalytic activity of BiOBr increases in the first stage and then decreases,which is related to good crystallization and three-dimensional structure.
文摘This paper represents the interaction of well characterized Lewis base [（Pyr）nCuX]4O2, n = 1 or 2, X = Cl, Br or I, Pyr = pyrrolidine with CO2 as a Lewis acid to produce new series of oxidative coupling and catechol oxidase initiators [（Pyr）nCuX]4（CO3）2. These carbonato derivatives are isolated as stable solids. They are easily soluble in aprotic solvents as CH2Cl2 or PhNO2. Cryoscopic measurements support tetranuclear core structure for all of them. Infrared spectra show differences from their oxo analogous in the carbonato domains but those differences did not distinguish between tridentate bridging carbonato and bidentate one. Rate of oxidation of 2,6-dimethylphenol （DMP） by [（Pyr）CuCl]4（CO3）2, supports coordination number six for Cu（Ⅱ） centers in [（Pyr）CuCl]4（CO3）2. In order to fulfill coordination number six, for n = 1, carbonate will act as tridentate while for n = 2, it will act as bidentate, as shown in Scheme 4. Near infrared spectra indicate a [（3 halo） Cu（Ⅱ） charge transfer] for [（Pyr）nCuX]4（CO3）2, n = 1 or 2, X = Cl or Br. Low molecular absorptivities of the maxima at 825 nm and 730 nm for [（Pyr）nCuI]4（CO3）2, n = 1 or 2 with a minimum of high molecular absorptivities at 600 nm, comparing to X= CI or Br analogous, support a step structure for [（Pyr）,Cul]4（CO3）2, as shown in Scheme 5. Cyclic voltammograms for [（Pyr）nCuX]4（CO3）2; n = 1 or 2, X = CI or Br, are irreversible in characters.
