The high-temperature(HT) and low-temperature(LT) hydrothermal stabilities of molecular-sieve-based catalysts are important for the selective catalytic reduction of NOx with ammonia(NH3-SCR). In this paper, we report a...The high-temperature(HT) and low-temperature(LT) hydrothermal stabilities of molecular-sieve-based catalysts are important for the selective catalytic reduction of NOx with ammonia(NH3-SCR). In this paper, we report a catalyst, Cu2+ loading SAPO-17, synthesized using cyclohexylamine(CHA), which is commercially available and inexpensive and is utilized in NH3-SCR reduction for the first time. After systematic investigations on the optimization of Si and Cu2+ contents, it was concluded that Cu-SAPO-17-8.0%-0.22 displays favorable catalytic performance, even after being heated at 353 K for 24 h and at 973 K for 16 h. Moreover, the locations of CHAs, host–guest interaction and the Bronsted acid sites were explored by Rietveld refinement against powder X-ray diffraction data of as-made SAPO-17-8.0%. The refinement results showed that two CHAs exist within one eri cage and that the protonated CHA forms a hydrogen bond with O4, which indicates that the proton bonding with O4 will form the Bronsted acid site after the calcination.展开更多
The significant decrease of acid sites caused by alkali metal poisoning is the major factor in the deactivation of commercial V_(2)O_(5)-WO_(3)/TiO_(2)NH_(3)-SCR catalysts.In this work,the solid superacid SO_(4)^(2-)-...The significant decrease of acid sites caused by alkali metal poisoning is the major factor in the deactivation of commercial V_(2)O_(5)-WO_(3)/TiO_(2)NH_(3)-SCR catalysts.In this work,the solid superacid SO_(4)^(2-)-TiO_(2) modified by sulfate radicals,was selected as the catalyst support,which showed superior potassium resistance.The physicochemical properties and K-poisoning resistance of the V_(2)O_(5)-WO_(3)/SO_(4)^(2-)-TiO_(2)(VWSTi) catalyst were carried out by XRD,BET,H2-TPR,NH3-TPD,XPS,in situ DRIFTS and TG.The results pointed out that the introduction of SO_(4)^(2-)significantly increased the NH3-SCR catalytic activity at high temperatures,with an exceptionally high NO_(x) conversion over 90% between 275℃ and 500℃.When 0.5%(mass) K_(2)O was doped on the catalysts,the catalytic performance of the traditional V_(2)O_(5)-WO_(3)/TiO_(2)(VWTi) catalyst decreased significantly,while the VWSTi catalyst could still maintain a NOxconversion over 90%in the range of 300–500℃.The characterizations suggested that the support of SO_(4)^(2-)-TiO_(2) greatly increased the number of acidic sites,thereby enhancing the adsorption capacity of the reactant NH_(3).The results above demonstrated a potential approach to achieve superior potassium resistance for NH3-SCR catalysts using solid superacid.展开更多
Copper-exchanged chabazite（Cu/CHA） catalysts have been found to be affected by alkali metal and alkaline earth ions. However, the effects of Na＋ ions on Cu/SAPO-34 for ammonia selective catalytic reduction（NH_3-SC...Copper-exchanged chabazite（Cu/CHA） catalysts have been found to be affected by alkali metal and alkaline earth ions. However, the effects of Na＋ ions on Cu/SAPO-34 for ammonia selective catalytic reduction（NH_3-SCR） are still unclear. In order to investigate the mechanism, five samples with various Na contents were synthesized and characterized. It was observed that the introduced Na＋ ion-exchanges with H＋and Cu2＋of Cu/SAPO-34. The exchange of H＋is easier than that of isolated Cu2＋. The exchanged Cu2＋ions aggregate and form ＂CuAl_2O4-like＂ species.The NH_3-SCR activity of Cu/SAPO-34 decreases with increasing Na content, and the loss of isolated Cu2＋and acid sites is responsible for the activity loss.展开更多
Lanthanum(La)ions are generally recognized to cause a decline of the catalytic performance for Cu-SSZ-13 zeolite in the selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR).Herein,we demonstrate that the NH_...Lanthanum(La)ions are generally recognized to cause a decline of the catalytic performance for Cu-SSZ-13 zeolite in the selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR).Herein,we demonstrate that the NH_(3)-SCR performance and hydrothermal stability of Cu-La-SSZ-13 zeolites can be enhanced with the incorporation of a small amount of La ions.The incorporation of La ions into SSZ-13 favors more Z_(2)Cu^(2+)ions at six-membered rings(6MRs),which results in higher hydrothermal stability of Cu-La-SSZ-13 than that of Cu-SSZ-13.The NO conversion of Cu-La-SSZ-13 achieves 5%–10%higher than that of Cu-SSZ-13 at the temperature range of 400–550℃ after hydrothermal ageing.While introducing excess amount of La ions in SSZ-13 may cause the formation of inactive CuO_(x),leading to the decrease of catalytic activity and hydrothermal stability.Notably,the low-temperature activity of Cu-SSZ-13 with a low Cu content(≤2 wt.%)can be boosted by the introduction of La ions,which is largely due to the improved redox ability of Cu active sites modified by La ions.Density functional theory(DFT)calculations indicate that La ions prefer to locate at eight-membered rings(8MRs)and thus promoting the formation of more Z_(2)Cu^(2+)ions.Meanwhile,the existence of La ions in SSZ-13 inhibits the dealumination process and the transformation from Z_(2)Cu^(2+)to CuO_(x),resulting in its enhanced hydrothermal stability.The present work sheds a new insight into the regulation of secondary metal cations for promoting high NH_(3)-SCR performance over Cu-SSZ-13 zeolite catalysts.展开更多
Mn-based catalysts have exhibited promising performance in low-temperature selective catalytic reduction of NOx with NH_(3)(NH_(3)-SCR).However,challenges such as H_(2)O-or SO_(2)-induced poisoning to these catalysts ...Mn-based catalysts have exhibited promising performance in low-temperature selective catalytic reduction of NOx with NH_(3)(NH_(3)-SCR).However,challenges such as H_(2)O-or SO_(2)-induced poisoning to these catalysts still remain.Herein,we report an efficient strategy to prepare the dual single-atom Ce-Ti/MnO_(2)catalyst via ball-milling and calcination processes to address these issues.Ce-Ti/MnO_(2)showed better catalytic performance with a higher NO conversion and enhanced H_(2)O-and SO_(2)-resistance at a lowtemperature window(100−150°C)than the MnO_(2),single-atom Ce/MnO_(2),and Ti/MnO_(2)catalysts.The in situ infrared Fourier transform spectroscopy analysis confirmed there is no competitive adsorption between NOx and H_(2)O over the Ce-Ti/MnO_(2)catalyst.The calculation results showed that the synergistic interaction of the neighboring Ce-Ti dual atoms as sacrificial sites weakens the ability of the active Mn sites for binding SO_(2)and H_(2)O but enhances their binding to NH_(3).The insight obtained in this work deepens the understanding of catalysis for NH_(3)-SCR.The synthesis strategy developed in this work is easily scaled up to commercialization and applicable to preparing other MnO_(2)-based single-atom catalysts.展开更多
文摘The high-temperature(HT) and low-temperature(LT) hydrothermal stabilities of molecular-sieve-based catalysts are important for the selective catalytic reduction of NOx with ammonia(NH3-SCR). In this paper, we report a catalyst, Cu2+ loading SAPO-17, synthesized using cyclohexylamine(CHA), which is commercially available and inexpensive and is utilized in NH3-SCR reduction for the first time. After systematic investigations on the optimization of Si and Cu2+ contents, it was concluded that Cu-SAPO-17-8.0%-0.22 displays favorable catalytic performance, even after being heated at 353 K for 24 h and at 973 K for 16 h. Moreover, the locations of CHAs, host–guest interaction and the Bronsted acid sites were explored by Rietveld refinement against powder X-ray diffraction data of as-made SAPO-17-8.0%. The refinement results showed that two CHAs exist within one eri cage and that the protonated CHA forms a hydrogen bond with O4, which indicates that the proton bonding with O4 will form the Bronsted acid site after the calcination.
基金supported by the National Natural Science Foundation of China (22108184)China Postdoctoral Science Foundation (2021TQ0221)+1 种基金the Sichuan Science and Technology Program (2021JDRC0117)Chengdu Science and Technology Program (2021-YF05-00378-SN)。
文摘The significant decrease of acid sites caused by alkali metal poisoning is the major factor in the deactivation of commercial V_(2)O_(5)-WO_(3)/TiO_(2)NH_(3)-SCR catalysts.In this work,the solid superacid SO_(4)^(2-)-TiO_(2) modified by sulfate radicals,was selected as the catalyst support,which showed superior potassium resistance.The physicochemical properties and K-poisoning resistance of the V_(2)O_(5)-WO_(3)/SO_(4)^(2-)-TiO_(2)(VWSTi) catalyst were carried out by XRD,BET,H2-TPR,NH3-TPD,XPS,in situ DRIFTS and TG.The results pointed out that the introduction of SO_(4)^(2-)significantly increased the NH3-SCR catalytic activity at high temperatures,with an exceptionally high NO_(x) conversion over 90% between 275℃ and 500℃.When 0.5%(mass) K_(2)O was doped on the catalysts,the catalytic performance of the traditional V_(2)O_(5)-WO_(3)/TiO_(2)(VWTi) catalyst decreased significantly,while the VWSTi catalyst could still maintain a NOxconversion over 90%in the range of 300–500℃.The characterizations suggested that the support of SO_(4)^(2-)-TiO_(2) greatly increased the number of acidic sites,thereby enhancing the adsorption capacity of the reactant NH_(3).The results above demonstrated a potential approach to achieve superior potassium resistance for NH3-SCR catalysts using solid superacid.
基金financially supported by the National Key Research and Development program(No.2017YFC0211302)the National Natural Science Foundation of China(No.21676195)+1 种基金the Science Fund of State Key Laboratory of Engine Reliability(No.skler-201714)finical support from GM Global Research&Development(No.GAC1539)
文摘Copper-exchanged chabazite（Cu/CHA） catalysts have been found to be affected by alkali metal and alkaline earth ions. However, the effects of Na＋ ions on Cu/SAPO-34 for ammonia selective catalytic reduction（NH_3-SCR） are still unclear. In order to investigate the mechanism, five samples with various Na contents were synthesized and characterized. It was observed that the introduced Na＋ ion-exchanges with H＋and Cu2＋of Cu/SAPO-34. The exchange of H＋is easier than that of isolated Cu2＋. The exchanged Cu2＋ions aggregate and form ＂CuAl_2O4-like＂ species.The NH_3-SCR activity of Cu/SAPO-34 decreases with increasing Na content, and the loss of isolated Cu2＋and acid sites is responsible for the activity loss.
基金the National Natural Science Foundation of China(Nos.22288101,21920102005,and 21835002)the 111 Project(No.B17020)for supporting this work.
文摘Lanthanum(La)ions are generally recognized to cause a decline of the catalytic performance for Cu-SSZ-13 zeolite in the selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR).Herein,we demonstrate that the NH_(3)-SCR performance and hydrothermal stability of Cu-La-SSZ-13 zeolites can be enhanced with the incorporation of a small amount of La ions.The incorporation of La ions into SSZ-13 favors more Z_(2)Cu^(2+)ions at six-membered rings(6MRs),which results in higher hydrothermal stability of Cu-La-SSZ-13 than that of Cu-SSZ-13.The NO conversion of Cu-La-SSZ-13 achieves 5%–10%higher than that of Cu-SSZ-13 at the temperature range of 400–550℃ after hydrothermal ageing.While introducing excess amount of La ions in SSZ-13 may cause the formation of inactive CuO_(x),leading to the decrease of catalytic activity and hydrothermal stability.Notably,the low-temperature activity of Cu-SSZ-13 with a low Cu content(≤2 wt.%)can be boosted by the introduction of La ions,which is largely due to the improved redox ability of Cu active sites modified by La ions.Density functional theory(DFT)calculations indicate that La ions prefer to locate at eight-membered rings(8MRs)and thus promoting the formation of more Z_(2)Cu^(2+)ions.Meanwhile,the existence of La ions in SSZ-13 inhibits the dealumination process and the transformation from Z_(2)Cu^(2+)to CuO_(x),resulting in its enhanced hydrothermal stability.The present work sheds a new insight into the regulation of secondary metal cations for promoting high NH_(3)-SCR performance over Cu-SSZ-13 zeolite catalysts.
基金We gratefully acknowledge the financial supports from the National Natural Science Foundation of China(Nos.52070180,51938014,and 21802054)the Science Research Project of the Ministry of Education of the Heilongjiang Province of China(No.145109102)+2 种基金the Beijing Chenxi Environmental Engineering Co.,Ltd.Z.Z.thanks the financial support of Guangdong Key discipline fund for this collaborationY.J.thanks the financial supports from the Outstanding Youth cultivation program of Beijing Technology and Business University(No.19008021144)Research Foundation for Advanced Talents of Beijing Technology and Business University(No.19008020159).
文摘Mn-based catalysts have exhibited promising performance in low-temperature selective catalytic reduction of NOx with NH_(3)(NH_(3)-SCR).However,challenges such as H_(2)O-or SO_(2)-induced poisoning to these catalysts still remain.Herein,we report an efficient strategy to prepare the dual single-atom Ce-Ti/MnO_(2)catalyst via ball-milling and calcination processes to address these issues.Ce-Ti/MnO_(2)showed better catalytic performance with a higher NO conversion and enhanced H_(2)O-and SO_(2)-resistance at a lowtemperature window(100−150°C)than the MnO_(2),single-atom Ce/MnO_(2),and Ti/MnO_(2)catalysts.The in situ infrared Fourier transform spectroscopy analysis confirmed there is no competitive adsorption between NOx and H_(2)O over the Ce-Ti/MnO_(2)catalyst.The calculation results showed that the synergistic interaction of the neighboring Ce-Ti dual atoms as sacrificial sites weakens the ability of the active Mn sites for binding SO_(2)and H_(2)O but enhances their binding to NH_(3).The insight obtained in this work deepens the understanding of catalysis for NH_(3)-SCR.The synthesis strategy developed in this work is easily scaled up to commercialization and applicable to preparing other MnO_(2)-based single-atom catalysts.
