The oxidative polycondensation reaction conditions of 2-[(2-hydroxyphenyliminomethylbenzylidene)amino- phenol](2-HPIMBAP)has been accomplished by using air O_2 and NaOCl oxidants in an aqueous alkaline medium between ...The oxidative polycondensation reaction conditions of 2-[(2-hydroxyphenyliminomethylbenzylidene)amino- phenol](2-HPIMBAP)has been accomplished by using air O_2 and NaOCl oxidants in an aqueous alkaline medium between 50-90℃.The optimum reaction conditions of the oxidative polycondensation and the main parameters of the process were established.At the optimum reaction conditions,yield of the products were found to be 67.72% and 61.49% for air O_2 and NaOCl oxidants respectively.The structures of the monomer ...展开更多
The optimum reaction conditions of the oxidative polycondensation of 2-(thien-2-yl-methylene)aminophenol (2-TMAP) has been accomplished by using air O_2,H_2O_2 and NaOCl oxidants in an aqueous alkaline medium between...The optimum reaction conditions of the oxidative polycondensation of 2-(thien-2-yl-methylene)aminophenol (2-TMAP) has been accomplished by using air O_2,H_2O_2 and NaOCl oxidants in an aqueous alkaline medium between 20℃and 90℃.The structures of the monomer and oligomer were confirmed by FT-IR,UV-Vis,~1H-NMR and ^(13)C-NMR and elemental analysis.TGA-DTA,size exclusion chromatography(SEC) techniques and solubility tests were applied for characterization.The ~1H-NMR and ^(13)C-NMR data show that the polymeriz...展开更多
The thermoelectric properties of Sr0.61Ba0.39Nb2O6-δ ceramics, reduced in different conditions, are investigated in the temperature range from 323 K to 1073 K. The electrical transport behaviors of the samples are do...The thermoelectric properties of Sr0.61Ba0.39Nb2O6-δ ceramics, reduced in different conditions, are investigated in the temperature range from 323 K to 1073 K. The electrical transport behaviors of the samples are dominated by the thermal-activated polaron hopping in the low temperature range, the Fermi glass behavior in the middle temperature range, and the Anderson localized behavior in the high temperature range. The thermal conductivity presents a plateau at high- temperatures, indicating a glass-like thermal conduction behavior. Both the thermoelectric power factor and the thermal conductivity increase with the increase of the degree of oxygen-reduction. Taking these two factors into account, the oxygen-reduction can still contribute to promoting the thermoelectric figure of merit. The highest ZT value is obtained to be -0.19 at 1073 K in the heaviest oxygen reduced sample.展开更多
The solid solutions Ce_(0.9)RE_(0.1)O_(2-δ)(RE=Pr, Nd,Sm, Gd, Dy) were prepared by sol-gel method. The XRD measurement shows that the solid solution is crystallized in cubic fluorite-type structure and the cell volum...The solid solutions Ce_(0.9)RE_(0.1)O_(2-δ)(RE=Pr, Nd,Sm, Gd, Dy) were prepared by sol-gel method. The XRD measurement shows that the solid solution is crystallized in cubic fluorite-type structure and the cell volume of Ce_(0.9)RE_(0.1)O_(2-δ) decreases with the increase of atomic number of RE. The ionic conduction for Ce_(0.9)RE_(0.1)O_(2-δ) was measured by impedance spectroscopy and Ce_(0.9)Pr_(0.1)O_(2-δ) has better conductivity. The linear thermal expansion of Ce_(0.9)RE_(0.1)O_(2-δ) decreases with the increase of atomic number of RE.展开更多
Antibiotic pollution in aqueous solutions seriously endangers the natural environment and public health.In this work,Mo-doped transition metal FeCo–Se metal aerogels(MAs)were investigated as bifunctional catalysts fo...Antibiotic pollution in aqueous solutions seriously endangers the natural environment and public health.In this work,Mo-doped transition metal FeCo–Se metal aerogels(MAs)were investigated as bifunctional catalysts for the removal of sulfamethazine(SMT)in solution.The optimal Mo_(0.3)Fe_(1)Co_(3)–Se catalyst can remove 97.7% of SMT within 60 min(SMT content:10 mg/L,current intensity:10 mA/cm 2).The unique porous cross-linked structure of aerogel confered the catalyst sufficient active sites and efficient mass transfer channels.For the anode,Mo_(0.3)Fe_(1)Co_(3)–Se MAs exhibits superior oxygen evolution reaction(OER)property,with an overpotential of only 235 mV(10 mA/cm 2).Compared with Fe_(1)Co_(3) MAs or Mo_(0.3)Fe_(1)Co_(3) MAs,density functional theory(DFT)demonstrated that the better catalytic capacity of Mo_(0.3)Fe_(1)Co_(3)–Se MAs is attributed to the doping of Mo species and selenization lowers the energy barrier for the*OOH to O_(2) step in the OER process.Excellent OER perfor-mance ensures the self-oxygenation in this system,avoiding the addition of air or oxygen in the traditional electro-Fenton process.For the cathode,Mo doping can lead to the lattice contraction and metallic character of CoSe_(2),which is beneficial to accelerate electron transfer.The adjacent Co active sites effectively adsorb*OOH and inhibit the breakage of the O–O bond.Rotating ring disk electrode(RRDE)test indicated that Mo_(0.3)Fe_(1)Co_(3)–Se MAs has an excellent 2e^(-)ORR activity with H_(2)O_(2) selectivity up to 88%,and the generated H_(2)O_(2) is activated by the adjacent Fe site through heterogeneous Fenton process to generate⋅OH.展开更多
Ceramic fuel cells hold an important position for the sustainable energy future using renewable energy sources with high efficiency.The design and synthesis of active materials,interface engineering and having capabil...Ceramic fuel cells hold an important position for the sustainable energy future using renewable energy sources with high efficiency.The design and synthesis of active materials,interface engineering and having capability of low operating temperature is considered as an important factor to further increase the power output and stability of ceramic fuel cell devices.A novel methodology has vital importance to develop new functionalities of existing materials by introducing new different effects.The built-in electric field(BIEF) is one of the most recently used approaches to improve charge transfer and ionic conductivity of solid oxide materials.Herein,we demonstrate gradient doping strategy in CeO_(2)-δstructure to produce BIEF effect and to modulate the proton transport effectively at the surface layer rather than bulk structure.The inclusions of La and Sr metal ions at the surface and Co-metal ions into bulk-layer of CeO_(2)form the gradiently doped structure.The gradient doping into CeO_(2)highly improves the proton transport properties through the surface layer by modifying the energy levels.Moreover,unbalanced charge distribution due to gradient doping produces built-in electric-field to provide extra driving force for protons transport through surface layer.The acquired gradiently doped fluorite structure exhibits remarkable proton conductivity of>0.2 S/cm,as a result ceramic fuel cell shows power output of>1000 mW/cm2while operating at 500℃.This unique work highlights the critical role of gradiently doped electrolyte in electrochemical conversion energy devices and offers new understanding and practices for sustainable energy future.展开更多
A novel route to comprehensive utilization of valuable elements such as Ti, A1, Si and Mg in Ti-bearing electric arc furnace molten slag （Ti-bearing EAF slag） was proposed. The route can be expressed as a three-step...A novel route to comprehensive utilization of valuable elements such as Ti, A1, Si and Mg in Ti-bearing electric arc furnace molten slag （Ti-bearing EAF slag） was proposed. The route can be expressed as a three-step process including alkali fusion, water leaching and acidolysis. Following these processes under the optimum conditions, the recovery ratios of TiO2, Al2O3, SiO2 and MgO were about 97.5, 93.5, 27.9 and 53.5%, respectively. Meanwhile, nanostructured TiO2, NaA zeolite and Mg（OH）2 fire retardant were synthesized simultaneously by using Ti-bearing EAF slag as raw materials. In addition, the photocatalytic activity of prepared nanostructured TiO2 and the adsorption property of obtained NaA zeolite were investigated. The results showed that the photodegradation efficiency of as-prepared TiO2 was 80% for rhodamine B and the adsorption efficiency of NaA zeolite was 61% for Cu2＋ under the optimum conditions.展开更多
A new soluble polymer on 2-[(2 E)-1-methyl-2-buten-1-yl]aniline and its copolymers with aniline basis have been synthesized in various molar ratios. For all samples, the electrical conductivity, morphology, solubility...A new soluble polymer on 2-[(2 E)-1-methyl-2-buten-1-yl]aniline and its copolymers with aniline basis have been synthesized in various molar ratios. For all samples, the electrical conductivity, morphology, solubility, electrochemical properties, as well as spectral and molecular mass characteristics have been studied, and a comparative analysis with polyaniline has been carried out. The substituent introduced into the aniline aromatic ring significantly improves the solubility in typical organic solvents of a high molecular weight product. The morphology of the test compounds depends on the co-monomer ratio. As the content of the substituted aniline in the initial mixture increases, the morphology of the polymer changes from the inherent polyaniline fibrous microstructure to the globular one with irregular substituted polyaniline shapes and sizes. Electrochemical study of the samples revealed that the higher the oxidation potential, the wider the band gap(ranging from 2.00 to 2.15). The electrical conductivity decreases in proportion to the increase in the substituted aniline concentration of the initial co-monomer mixture and amounts to 12.5–35.7 × 10~6 nSm.展开更多
基金This work was supported by the Canakkale Onsekiz Mart University Scientific Research Projects Commission for financial support(No.2007/20).
文摘The oxidative polycondensation reaction conditions of 2-[(2-hydroxyphenyliminomethylbenzylidene)amino- phenol](2-HPIMBAP)has been accomplished by using air O_2 and NaOCl oxidants in an aqueous alkaline medium between 50-90℃.The optimum reaction conditions of the oxidative polycondensation and the main parameters of the process were established.At the optimum reaction conditions,yield of the products were found to be 67.72% and 61.49% for air O_2 and NaOCl oxidants respectively.The structures of the monomer ...
基金supported by the Government Planning Organization(GPO2002K120170-7)TUBITAK GrantsCommission for a research grant(No.TBAG-105T428).
文摘The optimum reaction conditions of the oxidative polycondensation of 2-(thien-2-yl-methylene)aminophenol (2-TMAP) has been accomplished by using air O_2,H_2O_2 and NaOCl oxidants in an aqueous alkaline medium between 20℃and 90℃.The structures of the monomer and oligomer were confirmed by FT-IR,UV-Vis,~1H-NMR and ^(13)C-NMR and elemental analysis.TGA-DTA,size exclusion chromatography(SEC) techniques and solubility tests were applied for characterization.The ~1H-NMR and ^(13)C-NMR data show that the polymeriz...
基金Project supported by the National Basic Research Program of China(Grant No.2013CB632506)the National Natural Science Foundation of China(Grant Nos.51202132 and 51002087)
文摘The thermoelectric properties of Sr0.61Ba0.39Nb2O6-δ ceramics, reduced in different conditions, are investigated in the temperature range from 323 K to 1073 K. The electrical transport behaviors of the samples are dominated by the thermal-activated polaron hopping in the low temperature range, the Fermi glass behavior in the middle temperature range, and the Anderson localized behavior in the high temperature range. The thermal conductivity presents a plateau at high- temperatures, indicating a glass-like thermal conduction behavior. Both the thermoelectric power factor and the thermal conductivity increase with the increase of the degree of oxygen-reduction. Taking these two factors into account, the oxygen-reduction can still contribute to promoting the thermoelectric figure of merit. The highest ZT value is obtained to be -0.19 at 1073 K in the heaviest oxygen reduced sample.
文摘The solid solutions Ce_(0.9)RE_(0.1)O_(2-δ)(RE=Pr, Nd,Sm, Gd, Dy) were prepared by sol-gel method. The XRD measurement shows that the solid solution is crystallized in cubic fluorite-type structure and the cell volume of Ce_(0.9)RE_(0.1)O_(2-δ) decreases with the increase of atomic number of RE. The ionic conduction for Ce_(0.9)RE_(0.1)O_(2-δ) was measured by impedance spectroscopy and Ce_(0.9)Pr_(0.1)O_(2-δ) has better conductivity. The linear thermal expansion of Ce_(0.9)RE_(0.1)O_(2-δ) decreases with the increase of atomic number of RE.
基金Thanks for the support of the National Natural Science Foundation of China(No.21776308)in this work.
文摘Antibiotic pollution in aqueous solutions seriously endangers the natural environment and public health.In this work,Mo-doped transition metal FeCo–Se metal aerogels(MAs)were investigated as bifunctional catalysts for the removal of sulfamethazine(SMT)in solution.The optimal Mo_(0.3)Fe_(1)Co_(3)–Se catalyst can remove 97.7% of SMT within 60 min(SMT content:10 mg/L,current intensity:10 mA/cm 2).The unique porous cross-linked structure of aerogel confered the catalyst sufficient active sites and efficient mass transfer channels.For the anode,Mo_(0.3)Fe_(1)Co_(3)–Se MAs exhibits superior oxygen evolution reaction(OER)property,with an overpotential of only 235 mV(10 mA/cm 2).Compared with Fe_(1)Co_(3) MAs or Mo_(0.3)Fe_(1)Co_(3) MAs,density functional theory(DFT)demonstrated that the better catalytic capacity of Mo_(0.3)Fe_(1)Co_(3)–Se MAs is attributed to the doping of Mo species and selenization lowers the energy barrier for the*OOH to O_(2) step in the OER process.Excellent OER perfor-mance ensures the self-oxygenation in this system,avoiding the addition of air or oxygen in the traditional electro-Fenton process.For the cathode,Mo doping can lead to the lattice contraction and metallic character of CoSe_(2),which is beneficial to accelerate electron transfer.The adjacent Co active sites effectively adsorb*OOH and inhibit the breakage of the O–O bond.Rotating ring disk electrode(RRDE)test indicated that Mo_(0.3)Fe_(1)Co_(3)–Se MAs has an excellent 2e^(-)ORR activity with H_(2)O_(2) selectivity up to 88%,and the generated H_(2)O_(2) is activated by the adjacent Fe site through heterogeneous Fenton process to generate⋅OH.
基金Project supported by the Fundamental Research Funds for the Central Universities (3203002105A2,4303002184)Jiangsu Provincial Program (JSSCRC2021491)。
文摘Ceramic fuel cells hold an important position for the sustainable energy future using renewable energy sources with high efficiency.The design and synthesis of active materials,interface engineering and having capability of low operating temperature is considered as an important factor to further increase the power output and stability of ceramic fuel cell devices.A novel methodology has vital importance to develop new functionalities of existing materials by introducing new different effects.The built-in electric field(BIEF) is one of the most recently used approaches to improve charge transfer and ionic conductivity of solid oxide materials.Herein,we demonstrate gradient doping strategy in CeO_(2)-δstructure to produce BIEF effect and to modulate the proton transport effectively at the surface layer rather than bulk structure.The inclusions of La and Sr metal ions at the surface and Co-metal ions into bulk-layer of CeO_(2)form the gradiently doped structure.The gradient doping into CeO_(2)highly improves the proton transport properties through the surface layer by modifying the energy levels.Moreover,unbalanced charge distribution due to gradient doping produces built-in electric-field to provide extra driving force for protons transport through surface layer.The acquired gradiently doped fluorite structure exhibits remarkable proton conductivity of>0.2 S/cm,as a result ceramic fuel cell shows power output of>1000 mW/cm2while operating at 500℃.This unique work highlights the critical role of gradiently doped electrolyte in electrochemical conversion energy devices and offers new understanding and practices for sustainable energy future.
基金This study was supported by the National Natural Science Foundation of China （Nos. 51471122 and 51604202）, the China Postdoctoral Science Foundation （No. 2016M592397） and the Science and Technology Project of Guangdong Province （No. 2013B090600025）.
文摘A novel route to comprehensive utilization of valuable elements such as Ti, A1, Si and Mg in Ti-bearing electric arc furnace molten slag （Ti-bearing EAF slag） was proposed. The route can be expressed as a three-step process including alkali fusion, water leaching and acidolysis. Following these processes under the optimum conditions, the recovery ratios of TiO2, Al2O3, SiO2 and MgO were about 97.5, 93.5, 27.9 and 53.5%, respectively. Meanwhile, nanostructured TiO2, NaA zeolite and Mg（OH）2 fire retardant were synthesized simultaneously by using Ti-bearing EAF slag as raw materials. In addition, the photocatalytic activity of prepared nanostructured TiO2 and the adsorption property of obtained NaA zeolite were investigated. The results showed that the photodegradation efficiency of as-prepared TiO2 was 80% for rhodamine B and the adsorption efficiency of NaA zeolite was 61% for Cu2＋ under the optimum conditions.
基金carried out within the framework of the state task program (No. AAAA-A19-119020890014-7)
文摘A new soluble polymer on 2-[(2 E)-1-methyl-2-buten-1-yl]aniline and its copolymers with aniline basis have been synthesized in various molar ratios. For all samples, the electrical conductivity, morphology, solubility, electrochemical properties, as well as spectral and molecular mass characteristics have been studied, and a comparative analysis with polyaniline has been carried out. The substituent introduced into the aniline aromatic ring significantly improves the solubility in typical organic solvents of a high molecular weight product. The morphology of the test compounds depends on the co-monomer ratio. As the content of the substituted aniline in the initial mixture increases, the morphology of the polymer changes from the inherent polyaniline fibrous microstructure to the globular one with irregular substituted polyaniline shapes and sizes. Electrochemical study of the samples revealed that the higher the oxidation potential, the wider the band gap(ranging from 2.00 to 2.15). The electrical conductivity decreases in proportion to the increase in the substituted aniline concentration of the initial co-monomer mixture and amounts to 12.5–35.7 × 10~6 nSm.
