The 2024 anodized aluminum alloy film was sealed by KAl(SO_(4))_(2)solution and the effect of sealing on corrosion resistance was investigated by means of potentiodynamic polarization curves,electrochemical impedance ...The 2024 anodized aluminum alloy film was sealed by KAl(SO_(4))_(2)solution and the effect of sealing on corrosion resistance was investigated by means of potentiodynamic polarization curves,electrochemical impedance spectroscopy,and X-ray photoelectron spectroscopy.The experimental results show that the optimal parameters for KAl(SO_(4))_(2)sealing are 35℃,with the pH value of 8,the concentration of 8 g/L,and the sealing time of 3 min.The corrosion resistance of the KAl(SO_(4))_(2)sealed sample can be significantly improved than that of unsealed one,and is obviously superior to that of the conventional hydrothermal sealed sample.Furthermore,X-ray photoelectron spectroscopy demonstrates that more Al(OH)_(3)will be formed in the process of KAl(SO_(4))_(2)sealing,which will shrink the diameter of the microporous and therefore results in the excellent corrosion resistance.展开更多
The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1...The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1). the CPC-12 conversion at 310C over Ti(SO_4)_2 calcined at 350C remained about 98.5% during 360 h on stream. and the selectivity to by-products remained zero. The findings enlarged the scope of traditional catalyst systems for the CFCs decomposition.展开更多
Highly active solid superacid catalysts for n-butane isomerization, SZ/A1_2O_3-P, were prepared by supporting SO-(4-2)/ZrO2, (SZ) on y-A1_2O_3 carrier using a precipitation method. The activities of some catalysts wer...Highly active solid superacid catalysts for n-butane isomerization, SZ/A1_2O_3-P, were prepared by supporting SO-(4-2)/ZrO2, (SZ) on y-A1_2O_3 carrier using a precipitation method. The activities of some catalysts were enhanced significantly j The activity of the most active sample. 60%SZ/Al_2O3-P, was even about 2 times more active than that of the SZ catalyst.展开更多
A series of tungstate red phosphors K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)were successfully prepared by sol-gel method,and the effects of the introduction of Li^(+)and SO_(4)^(2-)on the fluorescence intensity and t...A series of tungstate red phosphors K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)were successfully prepared by sol-gel method,and the effects of the introduction of Li^(+)and SO_(4)^(2-)on the fluorescence intensity and thermal quenching properties of the prepared K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)phosphors were investigated.The X-ray diffraction data show that the prepared(Li^(+)and SO_(4)^(2-))-doped KEu(WO_(4))_(2)phosphors have a monoclinic tetragonal structure.In addition,the emission intensities of all the observed emission peaks change significantly with the increase of Li~+doping concentration,especially the intensity of the emission peaks at 615 nm fluctuated significantly and reached the maximum at x=0.3 and y=0.2.The K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)phosphors are found to have the highest fluorescence intensity at x=0.3 and y=0.2.Moreover,the K_(0.7)Li_(0.3)Eu(WO_(4))_(1.8)(SO_(4))_(0.2)phosphor has better thermal quenching properties and luminescence efficiency,and the experimental results indicates that the fluorescence intensity and thermal burst performance of KEu(WO_(4))_(2)red phosphor could be effectively improved by using low-cost bionic doping of Li^(+)and SO_(4)^(2-).展开更多
Commercial V_(2)O_(5)-based catalysts have been successfully applied in NH_(3) selective catalytic reduction(NH_(3)-SCR)of NO_(x) from power stations,but their poor alkali-resistance restrains the wider application in...Commercial V_(2)O_(5)-based catalysts have been successfully applied in NH_(3) selective catalytic reduction(NH_(3)-SCR)of NO_(x) from power stations,but their poor alkali-resistance restrains the wider application in nonelectrical industries.In this study,NO_(x) reduction against alkali poisoning over V_(2)O_(5)/TiO_(2) is greatly improved via Ce(SO_(4))_(2) modification.It has been originally demonstrated that Ce^(4+)-SO_(4)^(2−)pair sites play crucial roles in improving NO_(x) reduction against alkali poisoning over V_(2)O_(5)/TiO_(2) catalysts.The strong interaction between V species and Ce sites of Ce^(4+)-SO_(4)^(2−)pairs triggers the reaction between NH_(4)^(+) species and gaseous NO via Eley-Rideal(E-R)reaction pathway.After K-poisoning,the SO_(4)^(2−)sites of Ce^(4+)-SO_(4)^(2−)pairs as protective sites strongly bond with K and thus maintain the high reaction efficiency via the E-R reaction pathway.This work demonstrates an effective strategy to enhance NO_(x) reduction against alkali poisoning over catalysts via constructing Ce^(4+)-SO_(4)^(2−)pair sites,contributing to developing alkali-resistant SCR catalysts for practical application in nonelectrical industries.展开更多
In recent years,sodium-ion batteries(SIBs)have been considered as one of the most promising alternatives to lithium-ion batteries(LIBs).Here,a new Na-super-ionic conductor(NASICON)cathode material Na Fe_(2)PO_(4)(SO_(...In recent years,sodium-ion batteries(SIBs)have been considered as one of the most promising alternatives to lithium-ion batteries(LIBs).Here,a new Na-super-ionic conductor(NASICON)cathode material Na Fe_(2)PO_(4)(SO_(4))_(2)is successfully prepared through solid state method for SIBs.While the poor electronic conductivity of iron-based materials results in its poor rate and cycle performance.Then the electrochemical is effectively promoting via Ca^(2+)doping.Na_(0.84)Ca_(0.08)Fe_(2)PO_(4)(SO_(4))_(2)have achieved considerable electrochemical properties.The first discharge specific capacity is 121.6 m A h g^(-1)at 25 m A g^(-1)with the voltage platform(-3.1 V)corresponding to Fe^(2+/3+).After 100 cycles,the capacity retention is 55.1%.The excellent electrochemical performance is caused by some Na^(+)is substituted by Ca^(2+)and leading to the fast sodium kinetics,which is well proved by the powder X-ray diffraction pattern and well corresponding to the galvanostatic intermittent titration technique and cyclic voltammetry testing result(the diffusivity values are around at 10^(-12)cm^(2)s^(-1)).展开更多
Zn(CF_(3)SO_(3))_(2)as an electrolyte has been widely used to improve the electrochemical performance for ZIBs due to that the bulky CF_(3)SO_(3)-can reduce the solvation effect of Zn^(2+)and promote the ionic diffusi...Zn(CF_(3)SO_(3))_(2)as an electrolyte has been widely used to improve the electrochemical performance for ZIBs due to that the bulky CF_(3)SO_(3)-can reduce the solvation effect of Zn^(2+)and promote the ionic diffusion.Herein,we found that Zn(CF_(3)SO_(3))_(2)electrolyte can induce different electrochemical mechanisms from ZnSO_(4)electrolyte.Compared to the ZnSO^(4)electrolyte,the HNaV_(6)O_(16)·4H2_(O)electrode with Zn(CF_(3)SO_(3))_(2)electrolyte exhibits a high capacity of 444 mAh·g^(-1)at 500 mA·g^(-1)with a capacity retention of 92.3%after 80 cycles.Even,at a high rate of 5 Ag-1,the HNaV_(6)O_(16)·4H_(2)O electrode delivers an initial discharge capacity of 328 mAh·g^(-1)with a capacity retention of 93.7%after 1000 cycles.Differing from the mechanism with ZnSO4 electrolyte,the excellent cycle stability of HNaV_(6)O_(16)·4H_(2)Oelectrode can be attributed to the in-situ phase transformation to ZnxV_(2)O_(5)·nH_(2)O based on the co-intercalation of Zn^(2+)/H^(+).展开更多
基金Funded by the National Natural Science Foundation of China(No.12175107)the Natural Science Foundation of Nanjing University of Posts and Telecommunications(No.NY220030)
文摘The 2024 anodized aluminum alloy film was sealed by KAl(SO_(4))_(2)solution and the effect of sealing on corrosion resistance was investigated by means of potentiodynamic polarization curves,electrochemical impedance spectroscopy,and X-ray photoelectron spectroscopy.The experimental results show that the optimal parameters for KAl(SO_(4))_(2)sealing are 35℃,with the pH value of 8,the concentration of 8 g/L,and the sealing time of 3 min.The corrosion resistance of the KAl(SO_(4))_(2)sealed sample can be significantly improved than that of unsealed one,and is obviously superior to that of the conventional hydrothermal sealed sample.Furthermore,X-ray photoelectron spectroscopy demonstrates that more Al(OH)_(3)will be formed in the process of KAl(SO_(4))_(2)sealing,which will shrink the diameter of the microporous and therefore results in the excellent corrosion resistance.
文摘The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1). the CPC-12 conversion at 310C over Ti(SO_4)_2 calcined at 350C remained about 98.5% during 360 h on stream. and the selectivity to by-products remained zero. The findings enlarged the scope of traditional catalyst systems for the CFCs decomposition.
文摘Highly active solid superacid catalysts for n-butane isomerization, SZ/A1_2O_3-P, were prepared by supporting SO-(4-2)/ZrO2, (SZ) on y-A1_2O_3 carrier using a precipitation method. The activities of some catalysts were enhanced significantly j The activity of the most active sample. 60%SZ/Al_2O3-P, was even about 2 times more active than that of the SZ catalyst.
基金Funded by the Science and Technology Bureau of Chengdu City(No.2022-YF05-02119-SN)。
文摘A series of tungstate red phosphors K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)were successfully prepared by sol-gel method,and the effects of the introduction of Li^(+)and SO_(4)^(2-)on the fluorescence intensity and thermal quenching properties of the prepared K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)phosphors were investigated.The X-ray diffraction data show that the prepared(Li^(+)and SO_(4)^(2-))-doped KEu(WO_(4))_(2)phosphors have a monoclinic tetragonal structure.In addition,the emission intensities of all the observed emission peaks change significantly with the increase of Li~+doping concentration,especially the intensity of the emission peaks at 615 nm fluctuated significantly and reached the maximum at x=0.3 and y=0.2.The K_(1-x)Li_(x)Eu(WO_(4))_(2-y)(SO_(4))_(y)phosphors are found to have the highest fluorescence intensity at x=0.3 and y=0.2.Moreover,the K_(0.7)Li_(0.3)Eu(WO_(4))_(1.8)(SO_(4))_(0.2)phosphor has better thermal quenching properties and luminescence efficiency,and the experimental results indicates that the fluorescence intensity and thermal burst performance of KEu(WO_(4))_(2)red phosphor could be effectively improved by using low-cost bionic doping of Li^(+)and SO_(4)^(2-).
基金the National Natural Science Foundation of China(Nos.22125604,22106100,21976117)Shanghai Rising-Star Program(No.22QA1403700)+1 种基金Chenguang Program supported by Shanghai Education Development FoundationShanghai Municipal Education Commission(No.22Z00354).
文摘Commercial V_(2)O_(5)-based catalysts have been successfully applied in NH_(3) selective catalytic reduction(NH_(3)-SCR)of NO_(x) from power stations,but their poor alkali-resistance restrains the wider application in nonelectrical industries.In this study,NO_(x) reduction against alkali poisoning over V_(2)O_(5)/TiO_(2) is greatly improved via Ce(SO_(4))_(2) modification.It has been originally demonstrated that Ce^(4+)-SO_(4)^(2−)pair sites play crucial roles in improving NO_(x) reduction against alkali poisoning over V_(2)O_(5)/TiO_(2) catalysts.The strong interaction between V species and Ce sites of Ce^(4+)-SO_(4)^(2−)pairs triggers the reaction between NH_(4)^(+) species and gaseous NO via Eley-Rideal(E-R)reaction pathway.After K-poisoning,the SO_(4)^(2−)sites of Ce^(4+)-SO_(4)^(2−)pairs as protective sites strongly bond with K and thus maintain the high reaction efficiency via the E-R reaction pathway.This work demonstrates an effective strategy to enhance NO_(x) reduction against alkali poisoning over catalysts via constructing Ce^(4+)-SO_(4)^(2−)pair sites,contributing to developing alkali-resistant SCR catalysts for practical application in nonelectrical industries.
基金the National Natural Science Foundation of China(No.91963118)the Science Technology Program of Jilin Province(No.20200201066JC)+1 种基金the“13th Five-Year”Science and Technology Research from the Education Department of Jilin Province(No.JJKH20201179KJ)the 111 Project(No.B13013)。
文摘In recent years,sodium-ion batteries(SIBs)have been considered as one of the most promising alternatives to lithium-ion batteries(LIBs).Here,a new Na-super-ionic conductor(NASICON)cathode material Na Fe_(2)PO_(4)(SO_(4))_(2)is successfully prepared through solid state method for SIBs.While the poor electronic conductivity of iron-based materials results in its poor rate and cycle performance.Then the electrochemical is effectively promoting via Ca^(2+)doping.Na_(0.84)Ca_(0.08)Fe_(2)PO_(4)(SO_(4))_(2)have achieved considerable electrochemical properties.The first discharge specific capacity is 121.6 m A h g^(-1)at 25 m A g^(-1)with the voltage platform(-3.1 V)corresponding to Fe^(2+/3+).After 100 cycles,the capacity retention is 55.1%.The excellent electrochemical performance is caused by some Na^(+)is substituted by Ca^(2+)and leading to the fast sodium kinetics,which is well proved by the powder X-ray diffraction pattern and well corresponding to the galvanostatic intermittent titration technique and cyclic voltammetry testing result(the diffusivity values are around at 10^(-12)cm^(2)s^(-1)).
基金This study was financially supported by the National Natural Science Foundation of China(No.51772193)China Postdoctral Science Foundation(No.2019T250254).
文摘Zn(CF_(3)SO_(3))_(2)as an electrolyte has been widely used to improve the electrochemical performance for ZIBs due to that the bulky CF_(3)SO_(3)-can reduce the solvation effect of Zn^(2+)and promote the ionic diffusion.Herein,we found that Zn(CF_(3)SO_(3))_(2)electrolyte can induce different electrochemical mechanisms from ZnSO_(4)electrolyte.Compared to the ZnSO^(4)electrolyte,the HNaV_(6)O_(16)·4H2_(O)electrode with Zn(CF_(3)SO_(3))_(2)electrolyte exhibits a high capacity of 444 mAh·g^(-1)at 500 mA·g^(-1)with a capacity retention of 92.3%after 80 cycles.Even,at a high rate of 5 Ag-1,the HNaV_(6)O_(16)·4H_(2)O electrode delivers an initial discharge capacity of 328 mAh·g^(-1)with a capacity retention of 93.7%after 1000 cycles.Differing from the mechanism with ZnSO4 electrolyte,the excellent cycle stability of HNaV_(6)O_(16)·4H_(2)Oelectrode can be attributed to the in-situ phase transformation to ZnxV_(2)O_(5)·nH_(2)O based on the co-intercalation of Zn^(2+)/H^(+).
