In this work, a series of Cu-ZSM-5 catalysts with different SiO2/Al2O3 ratios(25, 50, 100 and200) were synthesized and investigated in n-butylamine catalytic degradation. The n-butylamine can be completely catalytic d...In this work, a series of Cu-ZSM-5 catalysts with different SiO2/Al2O3 ratios(25, 50, 100 and200) were synthesized and investigated in n-butylamine catalytic degradation. The n-butylamine can be completely catalytic degradation at 350 ℃ over all Cu-ZSM-5 catalysts. Moreover, Cu-ZSM-5(25) exhibited the highest selectivity to N2, exceeding 90% at 350 ℃. These samples were investigated in detail by several characterizations to illuminate the dependence of the catalytic performance on redox properties, Cu species, and acidity. The characterization results proved that the redox properties and chemisorption oxygen primarily affect n-butylamine conversion. N2 selectivity was impacted by the Bronsted acidity and the isolated Cu^2+ species. Meanwhile, the surface acid sites over Cu-ZSM-5 catalysts could influence the formation of Cu species. Furthermore, in situ diffuse reflectance infrared Fourier transform spectra was adopted to explore the reaction mechanism. The Cu-ZSM-5 catalysts are the most prospective catalysts for nitrogen-containing volatile organic compounds removal, and the results in this study could provide new insights into catalysts design for VOC catalytic oxidation.展开更多
The title compound (C5N5H41P2Mo5O30.5) was synthesized under hydrothermal condition and its crystal structure was determined by X-ray diffraction. It belongs to triclinic system, space group P , with a=9.9645(6), b=10...The title compound (C5N5H41P2Mo5O30.5) was synthesized under hydrothermal condition and its crystal structure was determined by X-ray diffraction. It belongs to triclinic system, space group P , with a=9.9645(6), b=10.8666(7), c=15.814(1)? α=71.482(3), β=88.528(2), γ=78.448(2)°, V=1589.4(2)3, Dc=2.510g/cm3, Z=2,μ=2.138mm-1,λ(MoKα) = 0.71073 ? F(000)=1180. The final R and wR were 0.0396 and 0.1052 for 6626 observed reflections with I ≥2σ(I), respectively. The result of the structure analysis indicates that the [Mo5O15(PO4) (HPO4)]5- anion in the title compound consists of five edge-sharing or corner-sharing MoO6 octahedra and two corner-sharing PO4 tetrahedra. Each MoO6 octahedron adopts distorted octahedral geometry.展开更多
A new molybdophosphate, (NH3CH2CH2NH3)2Mo5O15(HPO4)2 has been synthesized under hydrothermal conditions and structurally characterized by single crystal X ray diffractions. The compound crystallizes in the monoclinic,...A new molybdophosphate, (NH3CH2CH2NH3)2Mo5O15(HPO4)2 has been synthesized under hydrothermal conditions and structurally characterized by single crystal X ray diffractions. The compound crystallizes in the monoclinic, space group C2/c, a=1.7633(2)nm, b=1.00122(11) nm, c=1.37624(13)nm, β=96.974(5)°, V=2.4117(5)nm3, Z=4, Dc=2.853g·cm-3, μ(MoKα)=2.766mm-1, F(000)=1992. The structure contains the isolated polyanions of [Mo5O15(HPO4)2]4- units around which the portonated ethylenediamine ions are pos itioned. By hydrogen bond interactions the polyanions are interconnected to form a three dimensional network. Other characterizations by powder XRD, IR and thermal analysis are also described. CCDC: 206321.展开更多
The nickel‐based complex Ni‐CH3CH2NH2‐intercalated niobate layered perovskite Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was synthesized via a facile in situ chemical reaction method.Using ultrathin H1.78Sr0.78Bi0.22Nb2O7...The nickel‐based complex Ni‐CH3CH2NH2‐intercalated niobate layered perovskite Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was synthesized via a facile in situ chemical reaction method.Using ultrathin H1.78Sr0.78Bi0.22Nb2O7nanosheets and nickel acetate as precursors.The composition,structure,photophysical properties,and photocatalytic activity for H2production of Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7were studied systematically.The photocatalyst loaded with0.5wt%Ni exhibited the highest H2evolution rate of372.67μmo/h.This was0.54times higher than the activity of the H1.78Sr0.78Bi0.22Nb2O7nanosheets.The activity of the optimized Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was comparable to that of the Pt‐loaded sample under the same reaction conditions.The photocatalytic activity of the Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was mainly attributed to the excellent separation of photogenerated carriers,after formation of the intercalated complex Ni‐CH3CH2NH2.This study provides a facile strategy to synthesize a non‐precious metal‐loaded photocatalyst for H2production.展开更多
基金supported by the National Natural Science Foundation of China (Nos. 21477149,21677160,and 21707152)Beijing Municipal Science and Technology Commission (Nos. Z181100000118003 and Z181100005418011)。
文摘In this work, a series of Cu-ZSM-5 catalysts with different SiO2/Al2O3 ratios(25, 50, 100 and200) were synthesized and investigated in n-butylamine catalytic degradation. The n-butylamine can be completely catalytic degradation at 350 ℃ over all Cu-ZSM-5 catalysts. Moreover, Cu-ZSM-5(25) exhibited the highest selectivity to N2, exceeding 90% at 350 ℃. These samples were investigated in detail by several characterizations to illuminate the dependence of the catalytic performance on redox properties, Cu species, and acidity. The characterization results proved that the redox properties and chemisorption oxygen primarily affect n-butylamine conversion. N2 selectivity was impacted by the Bronsted acidity and the isolated Cu^2+ species. Meanwhile, the surface acid sites over Cu-ZSM-5 catalysts could influence the formation of Cu species. Furthermore, in situ diffuse reflectance infrared Fourier transform spectra was adopted to explore the reaction mechanism. The Cu-ZSM-5 catalysts are the most prospective catalysts for nitrogen-containing volatile organic compounds removal, and the results in this study could provide new insights into catalysts design for VOC catalytic oxidation.
基金The paper is financially supported by NSF of Fujian Province (JA00137) by FPNSFC(E0110013)
文摘The title compound (C5N5H41P2Mo5O30.5) was synthesized under hydrothermal condition and its crystal structure was determined by X-ray diffraction. It belongs to triclinic system, space group P , with a=9.9645(6), b=10.8666(7), c=15.814(1)? α=71.482(3), β=88.528(2), γ=78.448(2)°, V=1589.4(2)3, Dc=2.510g/cm3, Z=2,μ=2.138mm-1,λ(MoKα) = 0.71073 ? F(000)=1180. The final R and wR were 0.0396 and 0.1052 for 6626 observed reflections with I ≥2σ(I), respectively. The result of the structure analysis indicates that the [Mo5O15(PO4) (HPO4)]5- anion in the title compound consists of five edge-sharing or corner-sharing MoO6 octahedra and two corner-sharing PO4 tetrahedra. Each MoO6 octahedron adopts distorted octahedral geometry.
文摘A new molybdophosphate, (NH3CH2CH2NH3)2Mo5O15(HPO4)2 has been synthesized under hydrothermal conditions and structurally characterized by single crystal X ray diffractions. The compound crystallizes in the monoclinic, space group C2/c, a=1.7633(2)nm, b=1.00122(11) nm, c=1.37624(13)nm, β=96.974(5)°, V=2.4117(5)nm3, Z=4, Dc=2.853g·cm-3, μ(MoKα)=2.766mm-1, F(000)=1992. The structure contains the isolated polyanions of [Mo5O15(HPO4)2]4- units around which the portonated ethylenediamine ions are pos itioned. By hydrogen bond interactions the polyanions are interconnected to form a three dimensional network. Other characterizations by powder XRD, IR and thermal analysis are also described. CCDC: 206321.
基金supported by the National Natural Science Foundation of China(U1403193,21643012)~~
文摘The nickel‐based complex Ni‐CH3CH2NH2‐intercalated niobate layered perovskite Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was synthesized via a facile in situ chemical reaction method.Using ultrathin H1.78Sr0.78Bi0.22Nb2O7nanosheets and nickel acetate as precursors.The composition,structure,photophysical properties,and photocatalytic activity for H2production of Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7were studied systematically.The photocatalyst loaded with0.5wt%Ni exhibited the highest H2evolution rate of372.67μmo/h.This was0.54times higher than the activity of the H1.78Sr0.78Bi0.22Nb2O7nanosheets.The activity of the optimized Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was comparable to that of the Pt‐loaded sample under the same reaction conditions.The photocatalytic activity of the Ni‐CH3CH2NH2/H1.78Sr0.78Bi0.22Nb2O7was mainly attributed to the excellent separation of photogenerated carriers,after formation of the intercalated complex Ni‐CH3CH2NH2.This study provides a facile strategy to synthesize a non‐precious metal‐loaded photocatalyst for H2production.
