In this study, we will introduce the modified (G'/G<sup>2</sup>)-expansion method to explore some of the exact traveling wave solutions of some nonlinear partial differential equations namely, Phi-4 eq...In this study, we will introduce the modified (G'/G<sup>2</sup>)-expansion method to explore some of the exact traveling wave solutions of some nonlinear partial differential equations namely, Phi-4 equation, Joseph-Egri (TRLW) equation, and Calogro-Degasperis (CD) equation. As a result, we have obtained solutions for the equations expressed in terms of trigonometric, hyperbolic and rational functions. Moreover, some selected solutions are plotted using some specific values for the parameters.展开更多
LiMn_(2)O_(4)(LMO)electrochemical lithium-ion pump has gained widespread attention due to its green,high efficiency,and low energy consumption in selectively extracting lithium from brine.However,collapse of crystal s...LiMn_(2)O_(4)(LMO)electrochemical lithium-ion pump has gained widespread attention due to its green,high efficiency,and low energy consumption in selectively extracting lithium from brine.However,collapse of crystal structure and loss of lithium extraction capacity caused by Mn dissolution loss limits its industrialized application.Hence,a multifunctional coating was developed by depositing amorphous AlPO_(4)on the surface of LMO using sol-gel method.The characterization and electrochemical performance test provided insights into the mechanism of Li^(+)embedment and de-embedment and revealed that multifunctional AlPO_(4)can reconstruct the physical and chemical state of LMO surface to improve the interface hydrophilicity,promote the transport of Li^(+),strengthen cycle stability.Remarkably,after 20 cycles,the capacity retention rate of 0.5AP-LMO reached 93.6%with only 0.147%Mn dissolution loss.The average Li^(+)release capacity of 0.5AP-LMO//Ag system in simulated brine is 28.77 mg/(g h),which is 90.4%higher than LMO.Encouragingly,even in the more complex Zabuye real brine,0.5AP-LMO//Ag can still maintain excellent lithium extraction performance.These results indicate that the 0.5AP-LMO//Ag lithium-ion pump shows promising potential as a Li^(+)selective extraction system.展开更多
Electrochemical measurement and chemical immersion test are employed to investigate the inhibition mechanism of Na2MoO4 for carbon steel,which is studied in 55%LiBr＋0.07mol/L LiOH solution at high temperature.Testing...Electrochemical measurement and chemical immersion test are employed to investigate the inhibition mechanism of Na2MoO4 for carbon steel,which is studied in 55%LiBr＋0.07mol/L LiOH solution at high temperature.Testing results indicate that the passive film on carbon steel surface is mainly composed of Fe3O4,and Mo is involved in the process of film forming,in a form of MoO3 and MoO2.The parametric analysis of the evolving potential and the blend potential of MoO2 shows that Mo mainly exists as MoO2 in passive film when the concentration of Na2MoO4 is lower than 150 mg/L.While its concentration is greater than 150mg/L,it mainly exists as MoO3 inside the film and exists as MoO2 outside the film.MoO4^2- is deoxidized as MoO2 on the surface of carbon steel,which may impede the corrosion of active-site and raise the blend potential of carbon steel,and then MoO4^2- adsorbs onto the defects of the passive film and decompounds as MoO3 during the process of film forming.The electric field caused by different valence of Mo in passive film may retard the dissolution of carbon steel and lead to an increase in the polarization impedance and a decrease in hydrogen evolution.As a result,heavy concentrated Na2MoO4 solution（greater than 150mg/L）has excellent inhibition effect on carbon steel in LiBr solution.展开更多
Novel Bi2WO6-BiPO4 photocatalysts with heterojunction structure were fabricated through a facile hydrothermal route. The photocatalytic properties of Bi2WO6-BiPO4 composites were evaluated by photocatalytic degradatio...Novel Bi2WO6-BiPO4 photocatalysts with heterojunction structure were fabricated through a facile hydrothermal route. The photocatalytic properties of Bi2WO6-BiPO4 composites were evaluated by photocatalytic degradation of rhodamine B （Rh B） under simulated sunlight irradiation. The results showed that Bi2WO6-BiPO4 photocatalysts displayed much higher photocatalytic performances for Rh B degradation than the single BiPO4 and Bi2WO6. The best photocatalytic activity of Bi2WO6-BiPO4 with nearly 100% Rh B degradation located at molar ratio of 1：1 after 20 min irradiation. The enhanced photo-catalytic performance could be mainly ascribed to the formation of heterojunction interface in Bi2WO6-BiPO4 which facilitated the transfer and separation of photogenerated electron-hole pairs, as well as the strong visible light absorption originating from the sensitization role of Bi2WO6 to BiPO4. It was also found that the photodegradation of Rh B molecules was mainly attributed to the oxidation action of the generated O2^· - radicals and partly to the action of hvb^＋ via direct hole oxidation process.展开更多
Nanosphere-like Li2FeSiO4/C was synthesized via a solution method using sucrose as carbon sources under a mild condition of time-saving and energy-saving, followed by sintering at high temperatures for crystallization...Nanosphere-like Li2FeSiO4/C was synthesized via a solution method using sucrose as carbon sources under a mild condition of time-saving and energy-saving, followed by sintering at high temperatures for crystallization. The amount of carbon in the composite is less than 10% （mass fraction）, and the X-ray diffraction result confirms that the sample is of pure single phase indexed with the orthorhombic Pmn21 space group. The particle size of the Li2FeSiO4/C synthesized at 700 °C for 9 h is very fine and spherical-like with a size of 200 nm. The electrochemical performance of this material, including reversible capacity, cycle number, and charge-discharge characteristics, were tested. The cell of this sample can deliver a discharge capacity of 166 mA-h/g at C/20 rate in the first three cycles. After 30 cycles, the capacity decreases to 158 mA-h/g, and the capacity retention is up to 95%. The results show that this method can prepare nanosphere-like Li2FeSiO4/C composite with good electrochemical performance.展开更多
Along with the popularity of environmental protection concepts, the environmental treatment of water pollution attracts widespread attention, among which, the research on Bi-based semiconductor photocatalytic degradat...Along with the popularity of environmental protection concepts, the environmental treatment of water pollution attracts widespread attention, among which, the research on Bi-based semiconductor photocatalytic degradation technology has made great progress. However, the development of such bismuth-based composites still remains a challenging task due to difficult recovery and low catalytic efficiency. Herein, a novel CC/BiPO4</sub>/Bi2</sub>WO6</sub> composite was successfully synthesized through two-step hydrothermal method using activated flexible carbon cloth as a substrate. The results of the photocatalytic degradation experiments showed that the obtained CC/BiPO<sub>4</sub>/Bi<sub>2</sub>WO<sub>6</sub> composites can degrade 92.1% RhB in 60 min under UV-visible light irradiation, which was much higher than that of unloaded BiPO4</sub> (24.4%) and BiPO4</sub>/Bi2</sub>WO6</sub> (52.9%), exhibiting a better adsorption-photocatalytic degradation performance than BiPO4</sub> and BiPO4</sub>/Bi2</sub>WO6</sub>. Photoluminescence spectra indicated that the improved photocatalytic activity was due to the more effective inhibition of photogenerated carrier complexation. Furthermore, the radical capture experiments confirmed that h<sup>+</sup>, ·OH and O<sub>2</sub>-</sup> were the main active substances in the photocatalytic degradation process of RhB by the CC/BiPO4</sub>/Bi2</sub>WO6</sub> composites. More importantly, the prepared CC/BiPO4</sub>/Bi2</sub>WO6</sub> composite had a simple separation process and good recycling stability, and its photocatalytic degradation efficiency can still reach 53.3% after six cycles of RhB degradation. .展开更多
Normal photocatalysts cannot effectively remove low-concentration NO because of the high recombination rate of the photogenerated carriers.To overcome this problem,S-scheme composites have been developed to fabricate ...Normal photocatalysts cannot effectively remove low-concentration NO because of the high recombination rate of the photogenerated carriers.To overcome this problem,S-scheme composites have been developed to fabricate photocatalysts.Herein,a novel S-scheme Sb2WO6/g-C3N4 nanocomposite was fabricated by an ultrasound-assisted method,which exhibited excellent performance for photocatalytic ppb-level NO removal.Compared with the pure constituents of the nanocomposite,the as-prepared 15%-Sb2WO6/g-C3N4 photocatalyst could remove more than 68%continuous-flowing NO(initial concentration:400 ppb)under visible-light irradiation in 30 min.The findings of the trapping experiments confirmed that•O2^–and h+were the important active species in the NO oxidation reaction.Meanwhile,the transient photocurrent response and PL spectroscopy analyses proved that the unique S-scheme structure of the samples could enhance the charge separation efficiency.In situ DRIFTS revealed that the photocatalytic reaction pathway of NO removal over the Sb2WO6/g-C3N4 nanocomposite occurred via an oxygen-induced route.The present work proposes a new concept for fabricating efficient photocatalysts for photocatalytic ppb-level NO oxidation and provides deeper insights into the mechanism of photocatalytic NO oxidation.展开更多
Ag3PO4 is widely used in the field of photocatalysis because of its unique activity. However, photocorrosion limits its practical application. Therefore, it is very urgent to find a solution to improve the light corro...Ag3PO4 is widely used in the field of photocatalysis because of its unique activity. However, photocorrosion limits its practical application. Therefore, it is very urgent to find a solution to improve the light corrosion resistance of Ag3PO4. Herein, the Z-scheme WO3(H2O)0.333/Ag3PO4 composites are successfully prepared through microwave hydrothermal and simple stirring. The WO3(H2O)0.333/Ag3PO4 composites are characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis spectroscopy. In the degradation of organic pollutants, WO3(H2O)0.333/Ag3PO4 composites exhibit excellent performance under visible light. This is mainly attributed to the synergy of WO3(H2O)0.333 and Ag3PO4. Especially, the photocatalytic activity of 15%WO3(H2O)0.333/Ag3PO4 is the highest, and the methylene blue can be completely degraded in 4 min. In addition, the stability of the composites is also greatly enhanced. After five cycles of testing, the photocatalytic activity of 15%WO3(H2O)0.333/Ag3PO4 is not obviously decreased. However, the degradation efficiency of Ag3PO4 was only 20.2%. This indicates that adding WO3(H2O)0.333 can significantly improve the photoetching resistance of Ag3PO4. Finally, Z-scheme photocatalytic mechanism is investigated.展开更多
The effect of 2-butyne-1, 4-diol on silver electrodeposition process from 5, 5-dimethyl hydantoin solutions was investigated by means of cyclic voltammetric measurement, scanning electron microscopy (SEM) and X-ray di...The effect of 2-butyne-1, 4-diol on silver electrodeposition process from 5, 5-dimethyl hydantoin solutions was investigated by means of cyclic voltammetric measurement, scanning electron microscopy (SEM) and X-ray diffraction (XRD). Cyclic voltammetric studies indicate that the reduction process of silver electrodeposition is influenced by adding 2-butyne-1, 4-diol. Owing to its adsorption on the electrode surface, 2-butyne-1, 4-diol moderately hinders the mass transfer of the silver complexed ions from the bulk solution to the outer limit of the electrode double layer and affects the electrocrystallization step. Scanning electron microscopy analysis reveals that the presence of 2-butyne-1, 4-diol in the electrolyte is beneficial and the silver deposits obtained are smoother, more compact and more leveled. X-ray diffraction analysis of the silver deposits obtained at 0.5 g·L-1 2-butyne-1, 4-diol indicated that the (110) plane is the most preferred plane and is not affected by the presence of 2-butyne-1, 4-diol in the electrolyte.展开更多
In order to obtain better carbonation effect, extraction behavior of slag batch is necessary to study. Relevant parameters like selective extraction yield were originally discussed. The relationship between selective ...In order to obtain better carbonation effect, extraction behavior of slag batch is necessary to study. Relevant parameters like selective extraction yield were originally discussed. The relationship between selective extraction yield and conversion ratio was systemically focused on. The results show that alkaline earth metal conversion ratio is changed with leaching time and NH4CI concentration by first order exponential, and the maximum conversion for calcium keeps about 68% at 120 min in 0.4 mol/L NH4C1 solution, while leaching temperature and particle size have a linear effect on conversion ratio. Selective extraction yield of calcium is more than 93%, and the value of Mg is less than 5%. Apparent layer bands of silicon and calcium appear in the surface area through morphology detection of slag after leaching, and the case for 38-75 μm slag batch is more obvious than 75 150 μm slag and slag with larger particle size when leaching in 0.4 mol/L NH4Cl solution for 90 rain at 60 ℃.展开更多
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
Single-phaseα-CaSO4·0.5H2O whiskers were directly synthesized from waste Ca(NO3)2 solution using a hydrothermal method,and HNO3 was synchronously regenerated.The effects of reaction temperature and Ca^2+concentr...Single-phaseα-CaSO4·0.5H2O whiskers were directly synthesized from waste Ca(NO3)2 solution using a hydrothermal method,and HNO3 was synchronously regenerated.The effects of reaction temperature and Ca^2+concentration on the phase composition and morphology of products were determined by X-ray diffraction and optical microscopy.On the basis of the experimental results,the formation diagram ofα-CaSO4·0.5H2O was plotted within the range of 5–35 g·L^-1 Ca^2+and 115°C–150°C.In addition,the conditions of the direct synthesis ofα-CaSO4·0.5H2O were determined.Well-crystallized,single-phaseα-CaSO4·0.5H2O whiskers with high aspect ratios(length,1785μm;diameter,10.63μm;aspect ratio,168)and HNO3(70.25 g·L^-1)were obtained at the optimal conditions of 25 g·L^-1 Ca^2+and 125°C.展开更多
文摘In this study, we will introduce the modified (G'/G<sup>2</sup>)-expansion method to explore some of the exact traveling wave solutions of some nonlinear partial differential equations namely, Phi-4 equation, Joseph-Egri (TRLW) equation, and Calogro-Degasperis (CD) equation. As a result, we have obtained solutions for the equations expressed in terms of trigonometric, hyperbolic and rational functions. Moreover, some selected solutions are plotted using some specific values for the parameters.
基金supported by the National Natural Science Foundation of China(21908082,22278426,and 22178154)the Jiangsu Funding Program for Excellent Postdoctoral Talent(2022ZB629)+1 种基金the Natural Science Foundation of Jiangsu Province(BK20221367)the China Postdoctoral Science Foundation(2021M701472)。
文摘LiMn_(2)O_(4)(LMO)electrochemical lithium-ion pump has gained widespread attention due to its green,high efficiency,and low energy consumption in selectively extracting lithium from brine.However,collapse of crystal structure and loss of lithium extraction capacity caused by Mn dissolution loss limits its industrialized application.Hence,a multifunctional coating was developed by depositing amorphous AlPO_(4)on the surface of LMO using sol-gel method.The characterization and electrochemical performance test provided insights into the mechanism of Li^(+)embedment and de-embedment and revealed that multifunctional AlPO_(4)can reconstruct the physical and chemical state of LMO surface to improve the interface hydrophilicity,promote the transport of Li^(+),strengthen cycle stability.Remarkably,after 20 cycles,the capacity retention rate of 0.5AP-LMO reached 93.6%with only 0.147%Mn dissolution loss.The average Li^(+)release capacity of 0.5AP-LMO//Ag system in simulated brine is 28.77 mg/(g h),which is 90.4%higher than LMO.Encouragingly,even in the more complex Zabuye real brine,0.5AP-LMO//Ag can still maintain excellent lithium extraction performance.These results indicate that the 0.5AP-LMO//Ag lithium-ion pump shows promising potential as a Li^(+)selective extraction system.
文摘Electrochemical measurement and chemical immersion test are employed to investigate the inhibition mechanism of Na2MoO4 for carbon steel,which is studied in 55%LiBr＋0.07mol/L LiOH solution at high temperature.Testing results indicate that the passive film on carbon steel surface is mainly composed of Fe3O4,and Mo is involved in the process of film forming,in a form of MoO3 and MoO2.The parametric analysis of the evolving potential and the blend potential of MoO2 shows that Mo mainly exists as MoO2 in passive film when the concentration of Na2MoO4 is lower than 150 mg/L.While its concentration is greater than 150mg/L,it mainly exists as MoO3 inside the film and exists as MoO2 outside the film.MoO4^2- is deoxidized as MoO2 on the surface of carbon steel,which may impede the corrosion of active-site and raise the blend potential of carbon steel,and then MoO4^2- adsorbs onto the defects of the passive film and decompounds as MoO3 during the process of film forming.The electric field caused by different valence of Mo in passive film may retard the dissolution of carbon steel and lead to an increase in the polarization impedance and a decrease in hydrogen evolution.As a result,heavy concentrated Na2MoO4 solution（greater than 150mg/L）has excellent inhibition effect on carbon steel in LiBr solution.
基金Postdoctoral Science Foundation of China(2012M520605)Research Foundation of Taiyuan University of Technology(tyut-rc201369a,2013Z040)+1 种基金Open Foundation of State Key Laboratory of Coal Conversion(09-102)Natural Science Foundation of Shanxi Province(2013011042-1)
基金This work was supported by the National Natural Science Foundation of China （No.21407059） and the Science Development Project of Jilin Province （No.20130522071JH and No.20140101160JC）.
文摘Novel Bi2WO6-BiPO4 photocatalysts with heterojunction structure were fabricated through a facile hydrothermal route. The photocatalytic properties of Bi2WO6-BiPO4 composites were evaluated by photocatalytic degradation of rhodamine B （Rh B） under simulated sunlight irradiation. The results showed that Bi2WO6-BiPO4 photocatalysts displayed much higher photocatalytic performances for Rh B degradation than the single BiPO4 and Bi2WO6. The best photocatalytic activity of Bi2WO6-BiPO4 with nearly 100% Rh B degradation located at molar ratio of 1：1 after 20 min irradiation. The enhanced photo-catalytic performance could be mainly ascribed to the formation of heterojunction interface in Bi2WO6-BiPO4 which facilitated the transfer and separation of photogenerated electron-hole pairs, as well as the strong visible light absorption originating from the sensitization role of Bi2WO6 to BiPO4. It was also found that the photodegradation of Rh B molecules was mainly attributed to the oxidation action of the generated O2^· - radicals and partly to the action of hvb^＋ via direct hole oxidation process.
基金Project supported by Ministry of Education Key Laboratory of Synthetic and Natural Functional Molecular Chemistry, China Project (2010JK765) supported by the Education Department of Shaanxi Province, China
文摘Nanosphere-like Li2FeSiO4/C was synthesized via a solution method using sucrose as carbon sources under a mild condition of time-saving and energy-saving, followed by sintering at high temperatures for crystallization. The amount of carbon in the composite is less than 10% （mass fraction）, and the X-ray diffraction result confirms that the sample is of pure single phase indexed with the orthorhombic Pmn21 space group. The particle size of the Li2FeSiO4/C synthesized at 700 °C for 9 h is very fine and spherical-like with a size of 200 nm. The electrochemical performance of this material, including reversible capacity, cycle number, and charge-discharge characteristics, were tested. The cell of this sample can deliver a discharge capacity of 166 mA-h/g at C/20 rate in the first three cycles. After 30 cycles, the capacity decreases to 158 mA-h/g, and the capacity retention is up to 95%. The results show that this method can prepare nanosphere-like Li2FeSiO4/C composite with good electrochemical performance.
文摘Along with the popularity of environmental protection concepts, the environmental treatment of water pollution attracts widespread attention, among which, the research on Bi-based semiconductor photocatalytic degradation technology has made great progress. However, the development of such bismuth-based composites still remains a challenging task due to difficult recovery and low catalytic efficiency. Herein, a novel CC/BiPO4</sub>/Bi2</sub>WO6</sub> composite was successfully synthesized through two-step hydrothermal method using activated flexible carbon cloth as a substrate. The results of the photocatalytic degradation experiments showed that the obtained CC/BiPO<sub>4</sub>/Bi<sub>2</sub>WO<sub>6</sub> composites can degrade 92.1% RhB in 60 min under UV-visible light irradiation, which was much higher than that of unloaded BiPO4</sub> (24.4%) and BiPO4</sub>/Bi2</sub>WO6</sub> (52.9%), exhibiting a better adsorption-photocatalytic degradation performance than BiPO4</sub> and BiPO4</sub>/Bi2</sub>WO6</sub>. Photoluminescence spectra indicated that the improved photocatalytic activity was due to the more effective inhibition of photogenerated carrier complexation. Furthermore, the radical capture experiments confirmed that h<sup>+</sup>, ·OH and O<sub>2</sub>-</sup> were the main active substances in the photocatalytic degradation process of RhB by the CC/BiPO4</sub>/Bi2</sub>WO6</sub> composites. More importantly, the prepared CC/BiPO4</sub>/Bi2</sub>WO6</sub> composite had a simple separation process and good recycling stability, and its photocatalytic degradation efficiency can still reach 53.3% after six cycles of RhB degradation. .
文摘Normal photocatalysts cannot effectively remove low-concentration NO because of the high recombination rate of the photogenerated carriers.To overcome this problem,S-scheme composites have been developed to fabricate photocatalysts.Herein,a novel S-scheme Sb2WO6/g-C3N4 nanocomposite was fabricated by an ultrasound-assisted method,which exhibited excellent performance for photocatalytic ppb-level NO removal.Compared with the pure constituents of the nanocomposite,the as-prepared 15%-Sb2WO6/g-C3N4 photocatalyst could remove more than 68%continuous-flowing NO(initial concentration:400 ppb)under visible-light irradiation in 30 min.The findings of the trapping experiments confirmed that•O2^–and h+were the important active species in the NO oxidation reaction.Meanwhile,the transient photocurrent response and PL spectroscopy analyses proved that the unique S-scheme structure of the samples could enhance the charge separation efficiency.In situ DRIFTS revealed that the photocatalytic reaction pathway of NO removal over the Sb2WO6/g-C3N4 nanocomposite occurred via an oxygen-induced route.The present work proposes a new concept for fabricating efficient photocatalysts for photocatalytic ppb-level NO oxidation and provides deeper insights into the mechanism of photocatalytic NO oxidation.
基金supported by the National Natural Science Foundation of China(51572103 and 51502106)the Distinguished Young Scholar of Anhui Province(1808085J14)+2 种基金the Foundation for Young Talents in College of Anhui Province(gxyqZD2017051)the Key Foundation of Educational Commission of Anhui Province(KJ2016SD53)the Innovation Team of Design and Application of Advanced Energetic Materials(KJ2015TD003)~~
文摘Ag3PO4 is widely used in the field of photocatalysis because of its unique activity. However, photocorrosion limits its practical application. Therefore, it is very urgent to find a solution to improve the light corrosion resistance of Ag3PO4. Herein, the Z-scheme WO3(H2O)0.333/Ag3PO4 composites are successfully prepared through microwave hydrothermal and simple stirring. The WO3(H2O)0.333/Ag3PO4 composites are characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis spectroscopy. In the degradation of organic pollutants, WO3(H2O)0.333/Ag3PO4 composites exhibit excellent performance under visible light. This is mainly attributed to the synergy of WO3(H2O)0.333 and Ag3PO4. Especially, the photocatalytic activity of 15%WO3(H2O)0.333/Ag3PO4 is the highest, and the methylene blue can be completely degraded in 4 min. In addition, the stability of the composites is also greatly enhanced. After five cycles of testing, the photocatalytic activity of 15%WO3(H2O)0.333/Ag3PO4 is not obviously decreased. However, the degradation efficiency of Ag3PO4 was only 20.2%. This indicates that adding WO3(H2O)0.333 can significantly improve the photoetching resistance of Ag3PO4. Finally, Z-scheme photocatalytic mechanism is investigated.
文摘The effect of 2-butyne-1, 4-diol on silver electrodeposition process from 5, 5-dimethyl hydantoin solutions was investigated by means of cyclic voltammetric measurement, scanning electron microscopy (SEM) and X-ray diffraction (XRD). Cyclic voltammetric studies indicate that the reduction process of silver electrodeposition is influenced by adding 2-butyne-1, 4-diol. Owing to its adsorption on the electrode surface, 2-butyne-1, 4-diol moderately hinders the mass transfer of the silver complexed ions from the bulk solution to the outer limit of the electrode double layer and affects the electrocrystallization step. Scanning electron microscopy analysis reveals that the presence of 2-butyne-1, 4-diol in the electrolyte is beneficial and the silver deposits obtained are smoother, more compact and more leveled. X-ray diffraction analysis of the silver deposits obtained at 0.5 g·L-1 2-butyne-1, 4-diol indicated that the (110) plane is the most preferred plane and is not affected by the presence of 2-butyne-1, 4-diol in the electrolyte.
基金Project(2006BAE03A07)supported by National Key Technology Research and Development Program of 11th Five-year Plan of China
文摘In order to obtain better carbonation effect, extraction behavior of slag batch is necessary to study. Relevant parameters like selective extraction yield were originally discussed. The relationship between selective extraction yield and conversion ratio was systemically focused on. The results show that alkaline earth metal conversion ratio is changed with leaching time and NH4CI concentration by first order exponential, and the maximum conversion for calcium keeps about 68% at 120 min in 0.4 mol/L NH4C1 solution, while leaching temperature and particle size have a linear effect on conversion ratio. Selective extraction yield of calcium is more than 93%, and the value of Mg is less than 5%. Apparent layer bands of silicon and calcium appear in the surface area through morphology detection of slag after leaching, and the case for 38-75 μm slag batch is more obvious than 75 150 μm slag and slag with larger particle size when leaching in 0.4 mol/L NH4Cl solution for 90 rain at 60 ℃.
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.
基金supported by the Beijing Natural Science Foundation of China(2182040)the National Natural Science Foundation of China(51674026,U1802253)+1 种基金the Fundamental Research Funds for the Central Universities(FRF-TT-19-001)the China Scholarship Council(201906465004)。
文摘Single-phaseα-CaSO4·0.5H2O whiskers were directly synthesized from waste Ca(NO3)2 solution using a hydrothermal method,and HNO3 was synchronously regenerated.The effects of reaction temperature and Ca^2+concentration on the phase composition and morphology of products were determined by X-ray diffraction and optical microscopy.On the basis of the experimental results,the formation diagram ofα-CaSO4·0.5H2O was plotted within the range of 5–35 g·L^-1 Ca^2+and 115°C–150°C.In addition,the conditions of the direct synthesis ofα-CaSO4·0.5H2O were determined.Well-crystallized,single-phaseα-CaSO4·0.5H2O whiskers with high aspect ratios(length,1785μm;diameter,10.63μm;aspect ratio,168)and HNO3(70.25 g·L^-1)were obtained at the optimal conditions of 25 g·L^-1 Ca^2+and 125°C.
