In order to reduce the sulfur compounds in diesel fuel,boron nitride(BN)has been used as a novel metal-free catalyst in the present research.This nanocatalyst was synthesized via template-free approach followed by hea...In order to reduce the sulfur compounds in diesel fuel,boron nitride(BN)has been used as a novel metal-free catalyst in the present research.This nanocatalyst was synthesized via template-free approach followed by heating treatment at 900℃ in nitrogen atmosphere that the characteristics of the sample were identified by the X-ray diffraction,Fourier-transform infrared spectroscopy,Raman spectroscopy,field emission scanning electron microscopy,transmission electron microscopy,atomic force microscopy,and N2 adsorption-desorption isotherms.The results of structural and morphological analysis represented that BN has been successfully synthesized.The efficacy of the main operating parameters on the process was studied by using response surface methodology based on the Box-Behnken design method.The prepared catalyst showed high efficiency in oxidative desulfurization of diesel fuel with initial sulfur content of 8040 mg·kg^(-1)S.From statistical analysis,a significant quadratic model was obtained to predict the sulfur removal as a function of efficient parameters.The maximum efficiency of 72.4%was achieved under optimized conditions at oxidant/sulfur molar ratio of 10.2,temperature of 71℃,reaction time of 113 min,and catalyst dosage of 0.36 g.Also,the reusability of the BN was studied,and the result showed little reduction in activity of the catalyst after 10 times regeneration.Moreover,a plausible mechanism was proposed for oxidation of sulfur compounds on the surface of the catalyst.The present study shows that BN materials can be selected as promising metal-free catalysts for desulfurization process.展开更多
A series of ternary perovskite type oxides LaNi1-xCuxO3(x = 0.2,0.4,0.6,0.8,and 1.0) were synthesized via the sol-gel method in propionic acid.Partial substitution of Ni by Cu showed higher activities and selectivitie...A series of ternary perovskite type oxides LaNi1-xCuxO3(x = 0.2,0.4,0.6,0.8,and 1.0) were synthesized via the sol-gel method in propionic acid.Partial substitution of Ni by Cu showed higher activities and selectivities towards syngas products.LaNi0.8Cu0.2O3 was the most active toward the CH4 and CO2 conversions,and was selective for syngas products.Temperature-programmed reduction results showed that the addition of Cu facilitates the reduction of Ni3+ to Ni0,which is the main reason for the higher performance of this catalyst.展开更多
A novel Ag3PO4-CaO composite photocatalyst with enhanced photocatalytic activity was synthesized and utilized for degradation of ammonia from aqueous solution under sunlight. Ag3PO4 was prepared by pre- cipitation met...A novel Ag3PO4-CaO composite photocatalyst with enhanced photocatalytic activity was synthesized and utilized for degradation of ammonia from aqueous solution under sunlight. Ag3PO4 was prepared by pre- cipitation method, and the composite of AgjPO4-CaO was prepared via impregnation method. Utilization of eggshell for CaO synthesis provided a cost-effective and environmental friendly way for the hetero- geneous catalyst production. The as-prepared photocatalysts were characterized by FT-IR, FE-SEM, TEM, EDX, UV-vis and PL Results show that the Ag3PO4-CaO samples have excellent photocatalytic perfor- mances in the wide visible-light region. The effect of operating parameters like the content of Ag3PO4 in composite, initial ammonia concentration, pH of solution, catalyst dosage and oxygen supply was investi- gated. The photoeatalyst with 60 wt% content of Ag3PO4 had a high photocatalytic performance, because a low content of Ag3PO4 causes weak light absorption, and the excess amount of it results in serious electron-hole recombination due to the aggregation of AgjPO4 particles. The maximum ammonia degra- dation （about 70%） was achieved in 340 mg/L of ammonia, pH 11, and 1.25 g/L of catalyst in the presence of pure oxygen. In comparison to Ag3PO4, 60 wt% AgjPO4-CaO had a good stability and it could have been easily separated from the solution for recycling.展开更多
The catalytic performance of Mo supported on hierarchical alumina–silica(Si/Al = 15) with Mo loadings of 3, 6 and 15 wt% was investigated for the oxidative desulfurization(ODS) of model and real oil samples. Hierarch...The catalytic performance of Mo supported on hierarchical alumina–silica(Si/Al = 15) with Mo loadings of 3, 6 and 15 wt% was investigated for the oxidative desulfurization(ODS) of model and real oil samples. Hierarchical alumina–silica(h Al–Si) was synthesized by economical and ecofriendly silicate-1 seed-induced route using cetyltrimethylammonium bromide(CTAB) as mesoporogen. The effect of CTAB on the structure of catalyst was studied by characterization techniques. The results revealed that 6%Mo/h Al–Si had the highest sulfur removal compared to the other catalyst loadings. The effect of operating parameters was evaluated using Box–Behnken experimental design. The optimal desulfurization conditions with the 6%Mo/h Al–Si catalyst were determined at oxidation temperature of 67 ℃, oxidation time of 42 min, H2O2/S molar ratio of 8 and catalyst dosage of 0.008 g·ml^-1 for achieving a conversion of 95%. Under optimal conditions, different sulfur-containing compounds with initial concentration of 1000 ppm, Dibenzothiophene(DBT), Benzothiophene(BT) and Thiophen(Th), showed the catalytic oxidation reactivity in the order of DBT > BT>Th. According to the regeneration experiments, the 6%Mo/h Al–Si catalyst was reused 4 times with a little reduction in the performance. Also, the total sulfur content of gasoline and diesel after ODS process reached 156.6 and 4592.2 ppm, respectively.展开更多
In this work,a covalent organic framework(COF),which is constructed by the building blocks of[5,10,15,20-tetrakis(4-aminophenyl)porphinato]copper(Ⅱ)(CuTAPP)and p-benzaldehyde,is employed to integrate with TiO_(2) for...In this work,a covalent organic framework(COF),which is constructed by the building blocks of[5,10,15,20-tetrakis(4-aminophenyl)porphinato]copper(Ⅱ)(CuTAPP)and p-benzaldehyde,is employed to integrate with TiO_(2) for the purpose of establishing a Z-scheme hybrid.Within the system,isonicotinic acid performs the role of a bridge that connects the two components through a coordination bond.Further photocatalytic application reveals the hybrid framework is able to catalyze CO_(2) conversion under simulated solar light,resulting in CO production rate of 50.5 μmol g^(-1)·h^(-1),about 9.9 and 24.5 times that of COF and pristine TiO_(2),respectively.The ameliorated catalytic performance owes much to the por-phyrin block acting as photosensitizer that augments the light absorbance,and the establishment of Z-scheme system between the inorganic and orga nic comp on ents that enhances the separati on of the carriers.In addition,the chemical bridge also ensures a steady usage and stable charge delivery in the catalysis.Our study sheds light on the development of versatile approaches to covalently in corporate COFs with inorga nic semic on ductors.展开更多
文摘In order to reduce the sulfur compounds in diesel fuel,boron nitride(BN)has been used as a novel metal-free catalyst in the present research.This nanocatalyst was synthesized via template-free approach followed by heating treatment at 900℃ in nitrogen atmosphere that the characteristics of the sample were identified by the X-ray diffraction,Fourier-transform infrared spectroscopy,Raman spectroscopy,field emission scanning electron microscopy,transmission electron microscopy,atomic force microscopy,and N2 adsorption-desorption isotherms.The results of structural and morphological analysis represented that BN has been successfully synthesized.The efficacy of the main operating parameters on the process was studied by using response surface methodology based on the Box-Behnken design method.The prepared catalyst showed high efficiency in oxidative desulfurization of diesel fuel with initial sulfur content of 8040 mg·kg^(-1)S.From statistical analysis,a significant quadratic model was obtained to predict the sulfur removal as a function of efficient parameters.The maximum efficiency of 72.4%was achieved under optimized conditions at oxidant/sulfur molar ratio of 10.2,temperature of 71℃,reaction time of 113 min,and catalyst dosage of 0.36 g.Also,the reusability of the BN was studied,and the result showed little reduction in activity of the catalyst after 10 times regeneration.Moreover,a plausible mechanism was proposed for oxidation of sulfur compounds on the surface of the catalyst.The present study shows that BN materials can be selected as promising metal-free catalysts for desulfurization process.
文摘A series of ternary perovskite type oxides LaNi1-xCuxO3(x = 0.2,0.4,0.6,0.8,and 1.0) were synthesized via the sol-gel method in propionic acid.Partial substitution of Ni by Cu showed higher activities and selectivities towards syngas products.LaNi0.8Cu0.2O3 was the most active toward the CH4 and CO2 conversions,and was selective for syngas products.Temperature-programmed reduction results showed that the addition of Cu facilitates the reduction of Ni3+ to Ni0,which is the main reason for the higher performance of this catalyst.
文摘A novel Ag3PO4-CaO composite photocatalyst with enhanced photocatalytic activity was synthesized and utilized for degradation of ammonia from aqueous solution under sunlight. Ag3PO4 was prepared by pre- cipitation method, and the composite of AgjPO4-CaO was prepared via impregnation method. Utilization of eggshell for CaO synthesis provided a cost-effective and environmental friendly way for the hetero- geneous catalyst production. The as-prepared photocatalysts were characterized by FT-IR, FE-SEM, TEM, EDX, UV-vis and PL Results show that the Ag3PO4-CaO samples have excellent photocatalytic perfor- mances in the wide visible-light region. The effect of operating parameters like the content of Ag3PO4 in composite, initial ammonia concentration, pH of solution, catalyst dosage and oxygen supply was investi- gated. The photoeatalyst with 60 wt% content of Ag3PO4 had a high photocatalytic performance, because a low content of Ag3PO4 causes weak light absorption, and the excess amount of it results in serious electron-hole recombination due to the aggregation of AgjPO4 particles. The maximum ammonia degra- dation （about 70%） was achieved in 340 mg/L of ammonia, pH 11, and 1.25 g/L of catalyst in the presence of pure oxygen. In comparison to Ag3PO4, 60 wt% AgjPO4-CaO had a good stability and it could have been easily separated from the solution for recycling.
文摘The catalytic performance of Mo supported on hierarchical alumina–silica(Si/Al = 15) with Mo loadings of 3, 6 and 15 wt% was investigated for the oxidative desulfurization(ODS) of model and real oil samples. Hierarchical alumina–silica(h Al–Si) was synthesized by economical and ecofriendly silicate-1 seed-induced route using cetyltrimethylammonium bromide(CTAB) as mesoporogen. The effect of CTAB on the structure of catalyst was studied by characterization techniques. The results revealed that 6%Mo/h Al–Si had the highest sulfur removal compared to the other catalyst loadings. The effect of operating parameters was evaluated using Box–Behnken experimental design. The optimal desulfurization conditions with the 6%Mo/h Al–Si catalyst were determined at oxidation temperature of 67 ℃, oxidation time of 42 min, H2O2/S molar ratio of 8 and catalyst dosage of 0.008 g·ml^-1 for achieving a conversion of 95%. Under optimal conditions, different sulfur-containing compounds with initial concentration of 1000 ppm, Dibenzothiophene(DBT), Benzothiophene(BT) and Thiophen(Th), showed the catalytic oxidation reactivity in the order of DBT > BT>Th. According to the regeneration experiments, the 6%Mo/h Al–Si catalyst was reused 4 times with a little reduction in the performance. Also, the total sulfur content of gasoline and diesel after ODS process reached 156.6 and 4592.2 ppm, respectively.
基金financially supported by the National Natural Science Foundation of China (21663027 and 21808189)the Key Science and Technology Foundation of Gansu Province (20YF3GA021)+2 种基金the Innovation funding program of Universities of Gansu province (2020B-091)the Opening Project of Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education (LYJ18205)the Promotion Project of Young-Teacher Researchcapacity of Northwest Normal University (NWNU-LKQN-18-5).
文摘In this work,a covalent organic framework(COF),which is constructed by the building blocks of[5,10,15,20-tetrakis(4-aminophenyl)porphinato]copper(Ⅱ)(CuTAPP)and p-benzaldehyde,is employed to integrate with TiO_(2) for the purpose of establishing a Z-scheme hybrid.Within the system,isonicotinic acid performs the role of a bridge that connects the two components through a coordination bond.Further photocatalytic application reveals the hybrid framework is able to catalyze CO_(2) conversion under simulated solar light,resulting in CO production rate of 50.5 μmol g^(-1)·h^(-1),about 9.9 and 24.5 times that of COF and pristine TiO_(2),respectively.The ameliorated catalytic performance owes much to the por-phyrin block acting as photosensitizer that augments the light absorbance,and the establishment of Z-scheme system between the inorganic and orga nic comp on ents that enhances the separati on of the carriers.In addition,the chemical bridge also ensures a steady usage and stable charge delivery in the catalysis.Our study sheds light on the development of versatile approaches to covalently in corporate COFs with inorga nic semic on ductors.
