In this study, phosphorus modification by trimethyl phosphate impregnation was employed to enhance the hydrothermal stability of nano‐sized HZSM‐5 zeolites. A parallel modification was studied by ammonium dihydrogen...In this study, phosphorus modification by trimethyl phosphate impregnation was employed to enhance the hydrothermal stability of nano‐sized HZSM‐5 zeolites. A parallel modification was studied by ammonium dihydrogen phosphate impregnation. The modified zeolites were subjected to steam treatment at 800 °C for 4 h (100% steam) and employed as catalysts for olefin catalyticcracking (OCC) of full‐range fluid catalytic cracking (FCC) gasoline. X‐ray diffraction, N2 physicaladsorption and NH3 temperature‐programmed desorption analysis indicated that, although significantimprovements to the hydrothermal stability of nano‐sized HZSM‐5 zeolites can be observedwhen adopting both phosphorus modification strategies, impregnation with trimethyl phosphatedisplays further enhancement of the hydrothermal stability. This is because higher structural crystallinityis retained, larger specific surface areas/micropore volumes form, and there are greaternumbers of surface acid sites. Reaction experiments conducted using a fixed‐bed micro‐reactor(catalyst/oil ratio = 4, time on stream = 4 s) showed OCC of full‐range FCC gasoline-under a fluidized‐bed reaction mode configuration-to be a viable solution for the olefin problem of FCC gasoline.This reaction significantly decreased the olefin content in the full‐range FCC gasoline feed, andspecifically heavy‐end olefins, by converting the olefins into value‐added C2–C4 olefins and aromatics.At the same time, sulfide content of the gasoline decreased via a non‐hydrodesulfurization process.Nano‐sized HZSM‐5 zeolites modified with trimethyl phosphate exhibited enhanced catalytic performance for OCC of full‐range FCC gasoline.展开更多
Simultaneously achieving high activity,selectivity and stability for electrochemical CO_(2)reduction reaction(CO_(2)RR)remains great challenges.Herein,a phosphorus-modified Sn/Sn Oxcore/shell(P-Sn/SnO_x)catalyst,deriv...Simultaneously achieving high activity,selectivity and stability for electrochemical CO_(2)reduction reaction(CO_(2)RR)remains great challenges.Herein,a phosphorus-modified Sn/Sn Oxcore/shell(P-Sn/SnO_x)catalyst,derived from in situ electrochemical reduction of an amorphous Sn(HPO_(4))_(2) pre-catalyst,exhibits high CO_(2)RR performance.The total Faradaic efficiency(FE)of C_(1) products is close to 100%in a broad potential range from-0.49 to-1.02 V vs.reversible hydrogen electrode,and a total current density of 315.0 m A cm^(-2)is achieved.Moreover,the P-Sn/SnO_(x) catalyst maintains a formate FE of~90%for 120 h.Density functional theory calculations suggest that the phosphorus-modified Sn/SnO_(x) core/shell structure effectively facilitates formate production by enhancing CO_(2)adsorption and improving free energy profile of formate formation.展开更多
HZSM-5,with good surface acidity and shape selectivity,was reported as hydrocarbon cracking catalyst for multiple decades,however the hydrothermal stability,especially dealumination of tetrahedrally coordinated framew...HZSM-5,with good surface acidity and shape selectivity,was reported as hydrocarbon cracking catalyst for multiple decades,however the hydrothermal stability,especially dealumination of tetrahedrally coordinated framework aluminum(TFAl),has been proved extensively as one of the major challenges during reactionregeneration process.Phosphorus was proposed to stabilize TFAl and indeed it enhanced the hydrothermal stability.Unfortunately,most of the phosphorus species would remain outside of the zeolite pore,mainly as polyphosphate species,and block the micropore severely,with only a limited portion introduced into the channel being able to interact with TFAl.Enlarging the pore size by alkali treatment(desilication)is one of the most convinced methods,but the details about specific P species during alkali treatment and its transformation upon hydrothermal activation is not acquired,thus the mechanism has not been fully understood.Herein,the P-containing species and its transformation during direct P modification and acid/alkali treatment followed by Pmodification have been studied,and the mechanism on the interaction between P and Al species has been investigated,using several analytical methods,especially Solid-state nuclear magnetic resonance(SSNMR)spectroscopy.It was found that the combination of desilication and subsequent phosphorus modification can enhance the activity of the ZSM-5 for the cracking of ethylcyclohexane,due to the better hydrothermal stabilization of acid sites by the enhanced interaction between phosphorus and TFAl,resulting from the improved accessibility of TFAl because of the successful generation of mesoporosity.Whereas the acid treatment followed by phosphorus modification,with declined retention of crystallinity and P/Al ratio,monoclinic/orthorhombic transition during steam activation,and the failed generation of mesopores,would cause obvious aggregation of the phosphorus species and could not improve the hydrothermal stability of the ZSM-5 effectively,and the direct phosphatation turned out much worse.Finally,a specific index that the intensity of the signal at 39 in 27Al MAS NMR spectra before steam activation was proposed as the indicator for determining the efficiency of phosphorus modification.And the proposed mechanism on the interaction between phosphorus and TFAl during the phosphorus modification could also be applicable in other zeolites.展开更多
基金supported by the National Natural Science Foundation of China (21603023)the Petro China Innovation Foundation, China (2014D-5006-0501)~~
文摘In this study, phosphorus modification by trimethyl phosphate impregnation was employed to enhance the hydrothermal stability of nano‐sized HZSM‐5 zeolites. A parallel modification was studied by ammonium dihydrogen phosphate impregnation. The modified zeolites were subjected to steam treatment at 800 °C for 4 h (100% steam) and employed as catalysts for olefin catalyticcracking (OCC) of full‐range fluid catalytic cracking (FCC) gasoline. X‐ray diffraction, N2 physicaladsorption and NH3 temperature‐programmed desorption analysis indicated that, although significantimprovements to the hydrothermal stability of nano‐sized HZSM‐5 zeolites can be observedwhen adopting both phosphorus modification strategies, impregnation with trimethyl phosphatedisplays further enhancement of the hydrothermal stability. This is because higher structural crystallinityis retained, larger specific surface areas/micropore volumes form, and there are greaternumbers of surface acid sites. Reaction experiments conducted using a fixed‐bed micro‐reactor(catalyst/oil ratio = 4, time on stream = 4 s) showed OCC of full‐range FCC gasoline-under a fluidized‐bed reaction mode configuration-to be a viable solution for the olefin problem of FCC gasoline.This reaction significantly decreased the olefin content in the full‐range FCC gasoline feed, andspecifically heavy‐end olefins, by converting the olefins into value‐added C2–C4 olefins and aromatics.At the same time, sulfide content of the gasoline decreased via a non‐hydrodesulfurization process.Nano‐sized HZSM‐5 zeolites modified with trimethyl phosphate exhibited enhanced catalytic performance for OCC of full‐range FCC gasoline.
基金supported by the National Key R&D Program of China (2021YFA1501503)the National Natural Science Foundation of China (22125205,22002155,22002158,92045302)+5 种基金the“Transformational Technologies for Clean Energy and Demonstration”Strategic Priority Research Program of the Chinese Academy of Sciences (XDA21070613)the Fundamental Research Funds for the Central Universities (20720220008)the China Postdoctoral Science Foundation (2019M661142)the Natural Science Foundation of Liaoning Province (2021-MS-022)the High-Level Talents Innovation Project of Dalian City (2020RQ038)the support from the Photon Science Center for Carbon Neutrality。
文摘Simultaneously achieving high activity,selectivity and stability for electrochemical CO_(2)reduction reaction(CO_(2)RR)remains great challenges.Herein,a phosphorus-modified Sn/Sn Oxcore/shell(P-Sn/SnO_x)catalyst,derived from in situ electrochemical reduction of an amorphous Sn(HPO_(4))_(2) pre-catalyst,exhibits high CO_(2)RR performance.The total Faradaic efficiency(FE)of C_(1) products is close to 100%in a broad potential range from-0.49 to-1.02 V vs.reversible hydrogen electrode,and a total current density of 315.0 m A cm^(-2)is achieved.Moreover,the P-Sn/SnO_(x) catalyst maintains a formate FE of~90%for 120 h.Density functional theory calculations suggest that the phosphorus-modified Sn/SnO_(x) core/shell structure effectively facilitates formate production by enhancing CO_(2)adsorption and improving free energy profile of formate formation.
文摘HZSM-5,with good surface acidity and shape selectivity,was reported as hydrocarbon cracking catalyst for multiple decades,however the hydrothermal stability,especially dealumination of tetrahedrally coordinated framework aluminum(TFAl),has been proved extensively as one of the major challenges during reactionregeneration process.Phosphorus was proposed to stabilize TFAl and indeed it enhanced the hydrothermal stability.Unfortunately,most of the phosphorus species would remain outside of the zeolite pore,mainly as polyphosphate species,and block the micropore severely,with only a limited portion introduced into the channel being able to interact with TFAl.Enlarging the pore size by alkali treatment(desilication)is one of the most convinced methods,but the details about specific P species during alkali treatment and its transformation upon hydrothermal activation is not acquired,thus the mechanism has not been fully understood.Herein,the P-containing species and its transformation during direct P modification and acid/alkali treatment followed by Pmodification have been studied,and the mechanism on the interaction between P and Al species has been investigated,using several analytical methods,especially Solid-state nuclear magnetic resonance(SSNMR)spectroscopy.It was found that the combination of desilication and subsequent phosphorus modification can enhance the activity of the ZSM-5 for the cracking of ethylcyclohexane,due to the better hydrothermal stabilization of acid sites by the enhanced interaction between phosphorus and TFAl,resulting from the improved accessibility of TFAl because of the successful generation of mesoporosity.Whereas the acid treatment followed by phosphorus modification,with declined retention of crystallinity and P/Al ratio,monoclinic/orthorhombic transition during steam activation,and the failed generation of mesopores,would cause obvious aggregation of the phosphorus species and could not improve the hydrothermal stability of the ZSM-5 effectively,and the direct phosphatation turned out much worse.Finally,a specific index that the intensity of the signal at 39 in 27Al MAS NMR spectra before steam activation was proposed as the indicator for determining the efficiency of phosphorus modification.And the proposed mechanism on the interaction between phosphorus and TFAl during the phosphorus modification could also be applicable in other zeolites.
