The problem of water and sulfur poisoning in flue gas atmosphere remains a significant obstacle for low-temperature deNO_(x) catalysts.This study investigated the sulfation mechanism of the CoMn_(2)O_(4)/CeTiO_(x)(CMC...The problem of water and sulfur poisoning in flue gas atmosphere remains a significant obstacle for low-temperature deNO_(x) catalysts.This study investigated the sulfation mechanism of the CoMn_(2)O_(4)/CeTiO_(x)(CMCT)catalyst during the selective catalytic reduction of NO_(x) with NH3 under conditions containing H2O and SO_(2) at 150℃.Employing a comprehensive suite of time-resolved analysis and characterization techniques,the evolution of sulfate species was systematically categorized into three stages:initial rapid surface sulfate accumulation,the transformation of surface sulfates to bulk metal sulfates,and partial sulfates decomposition after the removal of H2O and SO_(2).These findings indicate that bulk metal sulfates irreversibly deactivate the catalyst by distorting active component lattices and consuming oxygen vacancies,whereas surface sulfates(including ammonium sulfates and surface-coordinated metal sulfates)cause reversible performance loss through decomposition.Furthermore,the competitive adsorption of H2O and SO_(2) significantly influences the catalytic efficiency,with H2O suppressing SO_(2) adsorption while simultaneously enhancing the formation of Brönsted acid sites.This research underscores the critical role of sulfate dynamics on catalyst performance,revealing the enhanced SO_(2) resistance of the Eley-Rideal mechanism facilitated by the Ce-Ti support relative to the Langmuir-Hinshelwood pathway.Collectively,the study unravels the complex interplay of sulfate dynamics influencing catalyst performance and provides potential approaches to mitigate deactivation in demanding atmospheric conditions.展开更多
Chemical vapor deposition is the predominant method to prepare MgAl_(2)O_(4)fibers.However,it faces several challenges,including exorbitantly high reaction temperatures,substantial production costs,and relatively low ...Chemical vapor deposition is the predominant method to prepare MgAl_(2)O_(4)fibers.However,it faces several challenges,including exorbitantly high reaction temperatures,substantial production costs,and relatively low yields.In this study,porous MgAl_(2)O_(4)fibers were fabricated through a solid-state reaction method,utilizing MgSO_(4)·5Mg(OH)_(2)·3H_(2)O whiskers as templates,mixed with either aluminum sol orα-Al_(2)O_(3)micropowder.The impact of various parameters on the synthesis of porous MgAl_(2)O_(4)fibres was systematically investigated,including the heat treatment temperature(1000,1100 and 1300℃),the holding time(3 and 10 h)and the aluminum source(aluminum sol orα-Al_(2)O_(3)micropowder).The results reveal that:(1)in comparison with fibers synthesized usingα-Al_(2)O_(3)as the aluminum source,those prepared with aluminum sol exhibit a significantly higher generation amount of MgAl_(2)O_(4);(2)as the heat treatment temperature increases,Al_(2)O_(3)gradually reacts with MgO,continuously increasing the formation amount of porous MgAl_(2)O_(4)with small and uniformly distributed nanopores,and the synthesized porous MgAl_(2)O_(4)fibres have small and uniform nanopores;(3)the optimal synthesis process involves using aluminum sol as the aluminum source and firing at 1300℃ for 3 h.展开更多
A microwave-H202 process for sludge pretreatment exhibited high efticiencies of releasing organics, nitrogen, and phosphorus, but large quantifies of H202 residues were detected. A uniform design method was thus emplo...A microwave-H202 process for sludge pretreatment exhibited high efticiencies of releasing organics, nitrogen, and phosphorus, but large quantifies of H202 residues were detected. A uniform design method was thus employed in this study to further optimize H202 dosage by investigating effects of pH and H202 dosage on the amount of 1-I202 residue and releases of organics, nitrogen, and phosphorus. A regression model was established with pH and H202 dosage as the independent variables, and H202 residue and releases of organics, nitrogen, and phosphorus as the dependent variables. In the optimized microwave-H202 process, the pH value of the sludge was firstly adjusted to 11.0, then the sludge was heated to 80~C and H202 was dosed at a H202 ：mixed liquor suspended solids （MLSS） ratio of 0.2, and the sludge was finally heated to 100~C by microwave irradiation. Compared to the microwave-H202 process without optimization, the H202 dosage and the utilization rate of H202 in the optimized microwave-H202 process were reduced by 80% and greatly improved by 3.87 times, respectively, when the H202：MLSS dosage ratio was decreased from 1.0 to 0.2, resulting in nearly the same release rate of soluble chemical oxygen demand in the microwave-H202 process without optimization at H202：MLSS ratio of 0.5.展开更多
The removal of four dissolved organic matter(DOM) fractions, non-acid hydrophobics,hydrophobic acids, hydrophilics and transphilics, was achieved by coagulation-UV/H_2O_2 oxidation in post-pharmaceutical wastewater(Ph...The removal of four dissolved organic matter(DOM) fractions, non-acid hydrophobics,hydrophobic acids, hydrophilics and transphilics, was achieved by coagulation-UV/H_2O_2 oxidation in post-pharmaceutical wastewater(PhW W). Coagulation with Polyferric chloride(PFC), Polymeric ferric sulfate(PFS) and Polymeric aluminum ferric chloride(PAFC) was studied separately to evaluate the effects of the initial pH and coagulant dosage. The coagulation-UV/H_2O_2 oxidation method resulted in much higher reduction rates for dissolved organic carbon(DOC)(by 75%) and UV_(254)(by 92%) than coagulation or UV/H_2O_2 oxidation alone. The proportion of non-acid hydrophobics, hydrophobic acids, transphilics and hydrophilics removed by coagulation was 54%, 49%, 27% and 12 %, while the combined treatment removed 92%, 87%,70% and 39%, respectively. Parallel factor analysis(PARAFAC) of fluorescence measurements revealed that the humic-like fluorescent component C4 showed the highest removal(by 44%)during the coagulation stage. After coagulation-UV/H_2O_2 treatment, the humic-like fluorescent component C3 had the highest removal(by 72%), whereas xenobiotic organic fluorescent components C1 and C4 remained recalcitrant to decomposition. Significant correlations(R2> 0.8)between C1 and the hydrophobic acids and non-acid hydrophobics suggested the possibility of using fluorescence spectroscopy as an effective tool to assess variations in DOM fraction treatment efficacy in coagulation-UV/H_2O_2 systems. After the combined treatment, toxic inhibition of cellular activity by post PhW W decreased from 88% to 47% and biodegradability increased from 0.1 to 0.52.展开更多
As an emerging preparation technology,wet chemical method has been employed widely to produce lots of alloy materials such as W and Mo based alloys,owing to its unique technical advantages.Ascertaining the synthesis m...As an emerging preparation technology,wet chemical method has been employed widely to produce lots of alloy materials such as W and Mo based alloys,owing to its unique technical advantages.Ascertaining the synthesis mechanism behind wet chemical method is indispensable for controlled synthesis of highquality W-Y2 O3 composite powder precursor.The co-deposition mechanism of yttrium and tungsten component behind the wet chemical method of preparing yttrium-doped tungsten composite nanopowder was investigated systematically in this work.A series of co-deposited composite powders fabricated under different acidity conditions were used as research targets for investigating the effect of surface composition and structure on co-deposition efficiency.It was found that white tungstic acid has more W-OH bonds and much higher co-deposition efficiency with Y^3+ions than yellow tungstic acid.It is illustrated that the coordination reaction between W-OH bonds on tungstic acid particles and Y^3+ions brings the co-deposition of yttrium and tungsten component into being.Through displacing H^+ions in W-OH bonds,Y^3+ions can be adsorbed on the surface of or incorporated into tungstic acid particles in form of ligand.Consequently,to control and regulate Y2 O3 content in powder precursor accurately,H^+ion concentration in wet chemical reaction should be in range of 0.55-2.82 mol L^-1 to obtain white tungstic acid.Besides,H^+ion concentration also has prominent effect on the grain size and morphology of reduced powder precursor.The optimal value should be around 1.58 mol L^-1,which can lead to minimum W grain size(about 17 nm) without bimodal structure.The chemical mechanism proposed in this work could produce great sense to preparation of high-quality precursor for sintering high-performance Y2 O3 dispersion strengthened W based alloys.Our work may also shed light on the approach to exploit analogous synthesis mechanism in other alloy systems.展开更多
The well-distributed, stable selenium nanoparticles (10 nm) with good adhesive ability and biocompatibility were successfully synthesized by using the template of chitosan cross-linked with glutaradehyde. The resulti...The well-distributed, stable selenium nanoparticles (10 nm) with good adhesive ability and biocompatibility were successfully synthesized by using the template of chitosan cross-linked with glutaradehyde. The resulting selenium nanoparticles were used as a new carrier for horseradish peroxidase to construct H2O2 biosensors with good performances.展开更多
Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest lumin...Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest luminescent sample synthesized at 600 oC.In relation to commercial sample,the relative luminescence intensity was 49.8%.The shape of emission spectrum of the sample thus changed and the charge-transfer-state band of excitation spectrum slightly shift toward higher energies.With increasing the anneal...展开更多
An efficient and convenient method for the synthesis of acyl-diazenes is reported. Ten acyl-diazenes have been synthesized from acylhydrazines in excellent yields under mild conditions. There are eight new substances...An efficient and convenient method for the synthesis of acyl-diazenes is reported. Ten acyl-diazenes have been synthesized from acylhydrazines in excellent yields under mild conditions. There are eight new substances among these compounds.展开更多
Long-lasting phosphor Y2O2S ： Eu^3＋ , Mg^2＋ , Ti^4＋ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased w...Long-lasting phosphor Y2O2S ： Eu^3＋ , Mg^2＋ , Ti^4＋ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased with the increase of Eu2O3 content in Y2O2S： Eu^3＋ （0.01 ≤ x ≤0.10）. On the other hand, the change of unit cell parameter a is not linear dependence. In the Y2O2S： Eu^3 ＋ crystal structure, Eu^3＋ ions only replaced Y^3 ＋ ions＇ places in which it posited center position of c axis. With the increase of Eu2O3 content, the position of the strongest emission peak changed from 540 nm （5D1→^ 7F2 transition） to 626 nm （^5Do→^7TF2 transition）, and the maximum intensity was obtained when x = 0.09 in Y2O2S： Eu^3＋ （0.01 ≤x ≤0.10）. This is due to the environment of trivalent europium in the crystal structure of Y2O2S. Doping with Mg^2＋ or Ti^4＋. ions alone cannot get the good long-lasting afterglow effect, whereas co-doping with Mg^2 ＋ and Ti^4 ＋ ions and excited with 365 nm ultraviolet light, a strong thermoluminesence peak appeared, red and orange long-lasting phosphorescence （LLP） was also observed and the phosphorescence lasted nearly 3 h in the light perception of the dark-adapted human eye （0.32 mcd·m^-2）. Thus the LLP mechanism was analyzed.展开更多
Novel red-emitting phosphors Sr2MgSi2O7：Eu3＋ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and flu...Novel red-emitting phosphors Sr2MgSi2O7：Eu3＋ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and fluorescence spectrophotometer, respectively. The results showed that the as-synthesized sample was Sr2MgSi2O7 with tetragonal crystal structure. The excitation spectrum of Sr2MgSi2O7：Eu3＋ was composed of two major parts： one was the broad band between 200 and 350 nm, which belonged to the charge transfer of Eu3＋-O2-; the other consisted of a series of sharp lines between 350 and 450 nm, ascribed to the f-f transition of Eu3＋. The emission spec-trum consisted of two emission peaks at 593 and 616 nm, which was attributed to 5D0→7F1 and 5D0→7F2 of Eu3＋, respectively. The concen-tration of Eu3＋ （x） had great effect on the emission intensity of Sr2-xMgSi2O7：Eu3＋x. When x varied in the range of 0.04-0.18, the intensity of emission peaks at 593 and 616 nm increased gradually with the concentration of Eu3＋ increasing. It was interesting that no concentration quenching occurred. Moreover, the luminescent intensity could be greatly enhanced with incorporation of charge compensator Li＋ ions.展开更多
The purpose of this work is to explore the effects of the introduction methods of Ce^4+and Zr^4+on the physicochemical properties,activity,and K tolerance of V2 O5-WO3/TiO2 catalyst for the selective catalytic reducti...The purpose of this work is to explore the effects of the introduction methods of Ce^4+and Zr^4+on the physicochemical properties,activity,and K tolerance of V2 O5-WO3/TiO2 catalyst for the selective catalytic reduction of NOx by NH3.Four different methods,namely pre-impregnation,post-impregnation,coimpregnation,and co-precipitation,were used to synthesize a series of V2 O5-WO3-TiO2-CeO2-ZrO2 catalysts.The catalysts were characterized by XRD,BET,NH3-TPD,XPS,and H2-TPR techniques.Moreover,the activity and anti-K poisoning performance were tested by an NH3-SCR model reaction.The results show that the introduction of Ce^4+and Zr^4+can improve the catalytic performance of V2O5-WO3/TiO2 catalyst,but the impregnation method cannot enhance the anti-K poisoning performance.Ce^4+and Zr^4+introduced by co-precipitation method can effectively improve the tolerance of K,which is mainly due to the incorporation of Ce^4+and Zr^4+into TiO2 lattice to form a uniform TiO2-CeO2-ZrO2 solid solution,resulting in the optimal surface acidity and redox performance,and reducing the decreases caused by Kpoisoning.Furthermore,based on the best introduction method,we further optimized the molar ratio of Ce^4+/Zr^4+,It is found that the catalyst exhibits the best anti-K poisoning performance when the molar ratio of Ce^4+/Zr^4+is 2:1.展开更多
Y2O3： Er^3＋, Yb^3＋ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980...Y2O3： Er^3＋, Yb^3＋ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm laser excitation. The results of XRD showed that the obtained Y2O3：Er^3＋,Yb^3＋ nanoparticles were of a cubic structure. The average crystallite sizes calculated were in the range of 28-40 nm. Green and red upconversion emission were observed, and attributed to ^2H11/2,^4S3/2→^4I15/2 and ^4F9/2→^4I15/2 transitions of the ion, respectively. The ratio of the intensity of green emission to that of red emission drastically changed with a change in the EDTA 2Na concentration. In the sample synthesized without EDTA, the relative intensity of the green emission was weaker than that of the red emission. The relative intensities of green emission increased with the increased amount of EDTA 2Na used. The possible upconversion luminescence mechanisms were discussed.展开更多
A series of Ceo.sFeo.30Zr0.20O2 catalysts were prepared by different methods （co-precipitations method, citric acid sol-gel method, impregnation method, physical mixed method, and hydrotherrnal method） and character...A series of Ceo.sFeo.30Zr0.20O2 catalysts were prepared by different methods （co-precipitations method, citric acid sol-gel method, impregnation method, physical mixed method, and hydrotherrnal method） and characterized by X-ray diffraction （XRD）, Raman spectroscopy, Brunauer-Emmett-Teller （BET） and H2-TPR measurements. Potential of the catalysts in the soot oxidation was evaluated in a temperature-programmed oxidation （TPO） apparatus. The results showed that all the Fe3＋ and Zr4＋ were incor- porated into ceria lattice to form a pure Ce-Fe-Zr-O solid solution for the co-precipitation sample, but two kinds of Fe phases ex- isted in the Ce-Fe-Zr-O catalysts prepared by other methods： Fe3＋ incorporated into CeO2 lattice and dispersed Fe2O3 clusters. The free Fe2O3 clusters could improve the activity of catalysts for soot oxidation comparing with the pure Ce-Fe-Zr-O solid solution owing to the synergetic effect between free Fe2O3 and surface oxygen vacancies. In addition, the activity of catalysts strongly relied on the surface reducibility of free Fe2O3 particles. Holding both abundant free Fe2O3 particles and high oxygen vacancy concentration, the hydrothermal Ce0.5Fe0.3Zr0.202 catalyst presented the lowest Ti （251℃, ignition temperature of soot oxidation） and Tm （310 ℃, maximum oxidation rate temperature） for soot combustion （with tight-contact between soot and catalysts） among the five samples. Even after aging at 800 ℃ for 10 h, the Ti and Tm were still relatively low, at 273 and 361 ℃, respectively, indicating high catalytic stability.展开更多
Proper utilization of the FeSO4·7H2O waste slag generated from TiO2 industry is an urgent need, and Fe3O4 particles are currently being widely used in the wastewater flocculation field. In this work, magnetite wa...Proper utilization of the FeSO4·7H2O waste slag generated from TiO2 industry is an urgent need, and Fe3O4 particles are currently being widely used in the wastewater flocculation field. In this work, magnetite was recovered from ferrous sulphate by a novel co-precipitation method with calcium hydroxide as the precipitant. Under optimum conditions, the obtained spherical magnetite particles are well crystallized with a Fe304 purity of 88.78%, but apt to aggregate with a median particle size of 1.83 μm. Magnetic measurement reveals the obtained Fe304 particles are soft magnetic with a saturation magnetization of 81.73 A-m2/kg. In addition, a highly crystallized gypsum co-product is obtained in blocky or irregular shape. Predictably, this study would provide additional opportunities for future application of low-cost Fe3O4 particles in water treatment field.展开更多
This study aims to examine the usability of environmentally harmless vegetable oil in the minimum quantity of lubrication(MQL)system in face milling of AISI O2 steel and to optimize the cutting parameters by different...This study aims to examine the usability of environmentally harmless vegetable oil in the minimum quantity of lubrication(MQL)system in face milling of AISI O2 steel and to optimize the cutting parameters by different statistical methods.Vegetable oil was preferred as cutting fluid,and Taguchi method was used in the preparation of the test pattern.After testing with the prepared test pattern,cutting performance in all parameters has been improved according to dry conditions thanks to the MQL system.The highest tool life was obtained by using cutting parameters of 7.5 m cutting length,100 m/min cutting speed,100 mL/h MQL flow rate and 0.1 mm/tooth feed rate.Optimum cutting parameters were determined according to the Taguchi analysis,and the obtained parameters were confirmed with the verification tests.In addition,the optimum test parameter was determined by applying the gray relational analysis method.After using ANOVA analysis according to the measured surface roughness and cutting force values,the most effective cutting parameter was observed to be the feed rate.In addition,the models for surface roughness and cutting force values were obtained with precisions of 99.63%and 99.68%,respectively.Effective wear mechanisms were found to be abrasion and adhesion.展开更多
文摘The problem of water and sulfur poisoning in flue gas atmosphere remains a significant obstacle for low-temperature deNO_(x) catalysts.This study investigated the sulfation mechanism of the CoMn_(2)O_(4)/CeTiO_(x)(CMCT)catalyst during the selective catalytic reduction of NO_(x) with NH3 under conditions containing H2O and SO_(2) at 150℃.Employing a comprehensive suite of time-resolved analysis and characterization techniques,the evolution of sulfate species was systematically categorized into three stages:initial rapid surface sulfate accumulation,the transformation of surface sulfates to bulk metal sulfates,and partial sulfates decomposition after the removal of H2O and SO_(2).These findings indicate that bulk metal sulfates irreversibly deactivate the catalyst by distorting active component lattices and consuming oxygen vacancies,whereas surface sulfates(including ammonium sulfates and surface-coordinated metal sulfates)cause reversible performance loss through decomposition.Furthermore,the competitive adsorption of H2O and SO_(2) significantly influences the catalytic efficiency,with H2O suppressing SO_(2) adsorption while simultaneously enhancing the formation of Brönsted acid sites.This research underscores the critical role of sulfate dynamics on catalyst performance,revealing the enhanced SO_(2) resistance of the Eley-Rideal mechanism facilitated by the Ce-Ti support relative to the Langmuir-Hinshelwood pathway.Collectively,the study unravels the complex interplay of sulfate dynamics influencing catalyst performance and provides potential approaches to mitigate deactivation in demanding atmospheric conditions.
文摘Chemical vapor deposition is the predominant method to prepare MgAl_(2)O_(4)fibers.However,it faces several challenges,including exorbitantly high reaction temperatures,substantial production costs,and relatively low yields.In this study,porous MgAl_(2)O_(4)fibers were fabricated through a solid-state reaction method,utilizing MgSO_(4)·5Mg(OH)_(2)·3H_(2)O whiskers as templates,mixed with either aluminum sol orα-Al_(2)O_(3)micropowder.The impact of various parameters on the synthesis of porous MgAl_(2)O_(4)fibres was systematically investigated,including the heat treatment temperature(1000,1100 and 1300℃),the holding time(3 and 10 h)and the aluminum source(aluminum sol orα-Al_(2)O_(3)micropowder).The results reveal that:(1)in comparison with fibers synthesized usingα-Al_(2)O_(3)as the aluminum source,those prepared with aluminum sol exhibit a significantly higher generation amount of MgAl_(2)O_(4);(2)as the heat treatment temperature increases,Al_(2)O_(3)gradually reacts with MgO,continuously increasing the formation amount of porous MgAl_(2)O_(4)with small and uniformly distributed nanopores,and the synthesized porous MgAl_(2)O_(4)fibres have small and uniform nanopores;(3)the optimal synthesis process involves using aluminum sol as the aluminum source and firing at 1300℃ for 3 h.
基金supported by the National Natural Science Foundation of China (No. 51008297)the Hi-Tech Research and Development Program (863) of China(No. 2007AA06Z347)the National Major Science & Technology Projects for Water Pollution Control and Management (No. 2012ZX07202-005)
文摘A microwave-H202 process for sludge pretreatment exhibited high efticiencies of releasing organics, nitrogen, and phosphorus, but large quantifies of H202 residues were detected. A uniform design method was thus employed in this study to further optimize H202 dosage by investigating effects of pH and H202 dosage on the amount of 1-I202 residue and releases of organics, nitrogen, and phosphorus. A regression model was established with pH and H202 dosage as the independent variables, and H202 residue and releases of organics, nitrogen, and phosphorus as the dependent variables. In the optimized microwave-H202 process, the pH value of the sludge was firstly adjusted to 11.0, then the sludge was heated to 80~C and H202 was dosed at a H202 ：mixed liquor suspended solids （MLSS） ratio of 0.2, and the sludge was finally heated to 100~C by microwave irradiation. Compared to the microwave-H202 process without optimization, the H202 dosage and the utilization rate of H202 in the optimized microwave-H202 process were reduced by 80% and greatly improved by 3.87 times, respectively, when the H202：MLSS dosage ratio was decreased from 1.0 to 0.2, resulting in nearly the same release rate of soluble chemical oxygen demand in the microwave-H202 process without optimization at H202：MLSS ratio of 0.5.
基金supported by the National Key Scientific and Technological Project for Water Pollution Control and Management (Nos.2012ZX07202-005,2012ZX07202-002,2014 ZX07216001-2)
文摘The removal of four dissolved organic matter(DOM) fractions, non-acid hydrophobics,hydrophobic acids, hydrophilics and transphilics, was achieved by coagulation-UV/H_2O_2 oxidation in post-pharmaceutical wastewater(PhW W). Coagulation with Polyferric chloride(PFC), Polymeric ferric sulfate(PFS) and Polymeric aluminum ferric chloride(PAFC) was studied separately to evaluate the effects of the initial pH and coagulant dosage. The coagulation-UV/H_2O_2 oxidation method resulted in much higher reduction rates for dissolved organic carbon(DOC)(by 75%) and UV_(254)(by 92%) than coagulation or UV/H_2O_2 oxidation alone. The proportion of non-acid hydrophobics, hydrophobic acids, transphilics and hydrophilics removed by coagulation was 54%, 49%, 27% and 12 %, while the combined treatment removed 92%, 87%,70% and 39%, respectively. Parallel factor analysis(PARAFAC) of fluorescence measurements revealed that the humic-like fluorescent component C4 showed the highest removal(by 44%)during the coagulation stage. After coagulation-UV/H_2O_2 treatment, the humic-like fluorescent component C3 had the highest removal(by 72%), whereas xenobiotic organic fluorescent components C1 and C4 remained recalcitrant to decomposition. Significant correlations(R2> 0.8)between C1 and the hydrophobic acids and non-acid hydrophobics suggested the possibility of using fluorescence spectroscopy as an effective tool to assess variations in DOM fraction treatment efficacy in coagulation-UV/H_2O_2 systems. After the combined treatment, toxic inhibition of cellular activity by post PhW W decreased from 88% to 47% and biodegradability increased from 0.1 to 0.52.
基金supported financially by the National Natural Science Foundation of China(Nos.51574178 and 51822404)the Natural Science Foundation of Tianjin(No.18JCYBJC17900)the Seed Foundation of Tianjin University(No.2018XRX-0005)。
文摘As an emerging preparation technology,wet chemical method has been employed widely to produce lots of alloy materials such as W and Mo based alloys,owing to its unique technical advantages.Ascertaining the synthesis mechanism behind wet chemical method is indispensable for controlled synthesis of highquality W-Y2 O3 composite powder precursor.The co-deposition mechanism of yttrium and tungsten component behind the wet chemical method of preparing yttrium-doped tungsten composite nanopowder was investigated systematically in this work.A series of co-deposited composite powders fabricated under different acidity conditions were used as research targets for investigating the effect of surface composition and structure on co-deposition efficiency.It was found that white tungstic acid has more W-OH bonds and much higher co-deposition efficiency with Y^3+ions than yellow tungstic acid.It is illustrated that the coordination reaction between W-OH bonds on tungstic acid particles and Y^3+ions brings the co-deposition of yttrium and tungsten component into being.Through displacing H^+ions in W-OH bonds,Y^3+ions can be adsorbed on the surface of or incorporated into tungstic acid particles in form of ligand.Consequently,to control and regulate Y2 O3 content in powder precursor accurately,H^+ion concentration in wet chemical reaction should be in range of 0.55-2.82 mol L^-1 to obtain white tungstic acid.Besides,H^+ion concentration also has prominent effect on the grain size and morphology of reduced powder precursor.The optimal value should be around 1.58 mol L^-1,which can lead to minimum W grain size(about 17 nm) without bimodal structure.The chemical mechanism proposed in this work could produce great sense to preparation of high-quality precursor for sintering high-performance Y2 O3 dispersion strengthened W based alloys.Our work may also shed light on the approach to exploit analogous synthesis mechanism in other alloy systems.
文摘The well-distributed, stable selenium nanoparticles (10 nm) with good adhesive ability and biocompatibility were successfully synthesized by using the template of chitosan cross-linked with glutaradehyde. The resulting selenium nanoparticles were used as a new carrier for horseradish peroxidase to construct H2O2 biosensors with good performances.
基金supported by the Ministry of Science and Technology of China (2006CB601104)the Foundation of International Joint Research of Beijing (2007N08)+1 种基金Natural Science Foundation of Jiangxi Province (2009GQC0042)Foundation of Jiangxi Educational Committee (GJJ10153)
文摘Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest luminescent sample synthesized at 600 oC.In relation to commercial sample,the relative luminescence intensity was 49.8%.The shape of emission spectrum of the sample thus changed and the charge-transfer-state band of excitation spectrum slightly shift toward higher energies.With increasing the anneal...
文摘An efficient and convenient method for the synthesis of acyl-diazenes is reported. Ten acyl-diazenes have been synthesized from acylhydrazines in excellent yields under mild conditions. There are eight new substances among these compounds.
文摘Long-lasting phosphor Y2O2S ： Eu^3＋ , Mg^2＋ , Ti^4＋ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased with the increase of Eu2O3 content in Y2O2S： Eu^3＋ （0.01 ≤ x ≤0.10）. On the other hand, the change of unit cell parameter a is not linear dependence. In the Y2O2S： Eu^3 ＋ crystal structure, Eu^3＋ ions only replaced Y^3 ＋ ions＇ places in which it posited center position of c axis. With the increase of Eu2O3 content, the position of the strongest emission peak changed from 540 nm （5D1→^ 7F2 transition） to 626 nm （^5Do→^7TF2 transition）, and the maximum intensity was obtained when x = 0.09 in Y2O2S： Eu^3＋ （0.01 ≤x ≤0.10）. This is due to the environment of trivalent europium in the crystal structure of Y2O2S. Doping with Mg^2＋ or Ti^4＋. ions alone cannot get the good long-lasting afterglow effect, whereas co-doping with Mg^2 ＋ and Ti^4 ＋ ions and excited with 365 nm ultraviolet light, a strong thermoluminesence peak appeared, red and orange long-lasting phosphorescence （LLP） was also observed and the phosphorescence lasted nearly 3 h in the light perception of the dark-adapted human eye （0.32 mcd·m^-2）. Thus the LLP mechanism was analyzed.
基金Project supported by the National Natural Science Foundation of China (20675023)
文摘Novel red-emitting phosphors Sr2MgSi2O7：Eu3＋ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and fluorescence spectrophotometer, respectively. The results showed that the as-synthesized sample was Sr2MgSi2O7 with tetragonal crystal structure. The excitation spectrum of Sr2MgSi2O7：Eu3＋ was composed of two major parts： one was the broad band between 200 and 350 nm, which belonged to the charge transfer of Eu3＋-O2-; the other consisted of a series of sharp lines between 350 and 450 nm, ascribed to the f-f transition of Eu3＋. The emission spec-trum consisted of two emission peaks at 593 and 616 nm, which was attributed to 5D0→7F1 and 5D0→7F2 of Eu3＋, respectively. The concen-tration of Eu3＋ （x） had great effect on the emission intensity of Sr2-xMgSi2O7：Eu3＋x. When x varied in the range of 0.04-0.18, the intensity of emission peaks at 593 and 616 nm increased gradually with the concentration of Eu3＋ increasing. It was interesting that no concentration quenching occurred. Moreover, the luminescent intensity could be greatly enhanced with incorporation of charge compensator Li＋ ions.
基金Project supported by the National Natural Science Foundation of China(21876168)the Key Projects for Common Key Technology Innovation in Key Industries in Chongqing(cstc2016zdcy-ztzx0020-01)+1 种基金Youth Innovation Promotion Association CAS(2019376)the Graduate Innovation Project of Chongqing Technology and Business University(yjscxx201803-028-22)。
文摘The purpose of this work is to explore the effects of the introduction methods of Ce^4+and Zr^4+on the physicochemical properties,activity,and K tolerance of V2 O5-WO3/TiO2 catalyst for the selective catalytic reduction of NOx by NH3.Four different methods,namely pre-impregnation,post-impregnation,coimpregnation,and co-precipitation,were used to synthesize a series of V2 O5-WO3-TiO2-CeO2-ZrO2 catalysts.The catalysts were characterized by XRD,BET,NH3-TPD,XPS,and H2-TPR techniques.Moreover,the activity and anti-K poisoning performance were tested by an NH3-SCR model reaction.The results show that the introduction of Ce^4+and Zr^4+can improve the catalytic performance of V2O5-WO3/TiO2 catalyst,but the impregnation method cannot enhance the anti-K poisoning performance.Ce^4+and Zr^4+introduced by co-precipitation method can effectively improve the tolerance of K,which is mainly due to the incorporation of Ce^4+and Zr^4+into TiO2 lattice to form a uniform TiO2-CeO2-ZrO2 solid solution,resulting in the optimal surface acidity and redox performance,and reducing the decreases caused by Kpoisoning.Furthermore,based on the best introduction method,we further optimized the molar ratio of Ce^4+/Zr^4+,It is found that the catalyst exhibits the best anti-K poisoning performance when the molar ratio of Ce^4+/Zr^4+is 2:1.
基金the Foundation for the University by Educational Department of Liaoning (05L337)Key Laboratory of Rare Earth Chemistry and Physics, Chinese Academy of Sciences
文摘Y2O3： Er^3＋, Yb^3＋ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm laser excitation. The results of XRD showed that the obtained Y2O3：Er^3＋,Yb^3＋ nanoparticles were of a cubic structure. The average crystallite sizes calculated were in the range of 28-40 nm. Green and red upconversion emission were observed, and attributed to ^2H11/2,^4S3/2→^4I15/2 and ^4F9/2→^4I15/2 transitions of the ion, respectively. The ratio of the intensity of green emission to that of red emission drastically changed with a change in the EDTA 2Na concentration. In the sample synthesized without EDTA, the relative intensity of the green emission was weaker than that of the red emission. The relative intensities of green emission increased with the increased amount of EDTA 2Na used. The possible upconversion luminescence mechanisms were discussed.
基金Project supported by National Natural Science Foundation of China(51374004,51204083,51174105,51104074)Natural Science Foundation of Yunnan Province(2010ZC018)
文摘A series of Ceo.sFeo.30Zr0.20O2 catalysts were prepared by different methods （co-precipitations method, citric acid sol-gel method, impregnation method, physical mixed method, and hydrotherrnal method） and characterized by X-ray diffraction （XRD）, Raman spectroscopy, Brunauer-Emmett-Teller （BET） and H2-TPR measurements. Potential of the catalysts in the soot oxidation was evaluated in a temperature-programmed oxidation （TPO） apparatus. The results showed that all the Fe3＋ and Zr4＋ were incor- porated into ceria lattice to form a pure Ce-Fe-Zr-O solid solution for the co-precipitation sample, but two kinds of Fe phases ex- isted in the Ce-Fe-Zr-O catalysts prepared by other methods： Fe3＋ incorporated into CeO2 lattice and dispersed Fe2O3 clusters. The free Fe2O3 clusters could improve the activity of catalysts for soot oxidation comparing with the pure Ce-Fe-Zr-O solid solution owing to the synergetic effect between free Fe2O3 and surface oxygen vacancies. In addition, the activity of catalysts strongly relied on the surface reducibility of free Fe2O3 particles. Holding both abundant free Fe2O3 particles and high oxygen vacancy concentration, the hydrothermal Ce0.5Fe0.3Zr0.202 catalyst presented the lowest Ti （251℃, ignition temperature of soot oxidation） and Tm （310 ℃, maximum oxidation rate temperature） for soot combustion （with tight-contact between soot and catalysts） among the five samples. Even after aging at 800 ℃ for 10 h, the Ti and Tm were still relatively low, at 273 and 361 ℃, respectively, indicating high catalytic stability.
基金Project(2013A090100013)supported by the Special Project on the Integration of Industry,Education and Research of Guangdong Province,ChinaProject(201407300993)supported by the High-Tech Research and Development Program of Xinjiang Uygur Autonomous Region,China
文摘Proper utilization of the FeSO4·7H2O waste slag generated from TiO2 industry is an urgent need, and Fe3O4 particles are currently being widely used in the wastewater flocculation field. In this work, magnetite was recovered from ferrous sulphate by a novel co-precipitation method with calcium hydroxide as the precipitant. Under optimum conditions, the obtained spherical magnetite particles are well crystallized with a Fe304 purity of 88.78%, but apt to aggregate with a median particle size of 1.83 μm. Magnetic measurement reveals the obtained Fe304 particles are soft magnetic with a saturation magnetization of 81.73 A-m2/kg. In addition, a highly crystallized gypsum co-product is obtained in blocky or irregular shape. Predictably, this study would provide additional opportunities for future application of low-cost Fe3O4 particles in water treatment field.
文摘This study aims to examine the usability of environmentally harmless vegetable oil in the minimum quantity of lubrication(MQL)system in face milling of AISI O2 steel and to optimize the cutting parameters by different statistical methods.Vegetable oil was preferred as cutting fluid,and Taguchi method was used in the preparation of the test pattern.After testing with the prepared test pattern,cutting performance in all parameters has been improved according to dry conditions thanks to the MQL system.The highest tool life was obtained by using cutting parameters of 7.5 m cutting length,100 m/min cutting speed,100 mL/h MQL flow rate and 0.1 mm/tooth feed rate.Optimum cutting parameters were determined according to the Taguchi analysis,and the obtained parameters were confirmed with the verification tests.In addition,the optimum test parameter was determined by applying the gray relational analysis method.After using ANOVA analysis according to the measured surface roughness and cutting force values,the most effective cutting parameter was observed to be the feed rate.In addition,the models for surface roughness and cutting force values were obtained with precisions of 99.63%and 99.68%,respectively.Effective wear mechanisms were found to be abrasion and adhesion.
