Silver-ceramics (Ag2MO2)(M=Co, Ni, or Cu) were prepared through thermal decompositionof coprecipitated oxalates. Pellets of these materials were annealed at 350℃ for different timeperiods up to 5 h. The effect of ann...Silver-ceramics (Ag2MO2)(M=Co, Ni, or Cu) were prepared through thermal decompositionof coprecipitated oxalates. Pellets of these materials were annealed at 350℃ for different timeperiods up to 5 h. The effect of annealing time on the transport properties was studied. IR andX-ray spectra were also studied.展开更多
The effects of potassium addition and the potassium content on the activity and selectivity of coprecipitated iron catalyst for Fischer-Tropsch synthesis （FTS） were studied in a fixed bed reactor at 1.5 MPa, 300 ℃,...The effects of potassium addition and the potassium content on the activity and selectivity of coprecipitated iron catalyst for Fischer-Tropsch synthesis （FTS） were studied in a fixed bed reactor at 1.5 MPa, 300 ℃, and contact time （W/F） of 12.5 gcath/mol using the model bio-oil-syngas of H2/CO/CO2/N2 （62/8/25/5, vol%）. It was found that potassium addition increases the catalyst activity for FTS and the reverse water gas shift reaction. Moreover, potassium increases the average molecular weight （chain length） of the hydrocarbon products. With the increase of potassium content, it was found that CH4 selectivity decreases and the selectivity of liquid phase products （C5＋） increases. The characteristics of FTS catalysts with different potassium content were also investigated by various characterization measurements including X-ray diffraction, X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller surface area. Based on experimental results, 100Fe/6Cu/16Al/6K （weight ratio） was selected as the optimal catalyst for FTS from bio-oil-syngas. The results indicate that the 100Fe/6Cu/16Al/6K catalyst is one of the most promising candidates to directly synthesize liquid bio-fuel using bio-oil-syngas.展开更多
In sulfidic anoxic environments,iron sulfides are widespread solid phases that play an important role in the arsenic(As)biogeochemical cycle.This work investigated the transformation process of FeS-As coprecipitates,t...In sulfidic anoxic environments,iron sulfides are widespread solid phases that play an important role in the arsenic(As)biogeochemical cycle.This work investigated the transformation process of FeS-As coprecipitates,the concurrent behavior,and the speciation of associated As under anoxic conditions.The results showed that FeS-As coprecipitates could convert to greigite and pyrite.The transformation degree of the produced solid phases was dependent upon the pH conditions and initial As species.These results showed that the As mobilization was closely associated with the solid phase transformation.The solid phase transformationwent from disordered mackinawite to crystallinemackinawite,then greigite and finally pyrite.The As in the coprecipitates underwent a process of release,fixation,and release again.Both reduction of As(Ⅴ)and oxidation of As(Ⅲ)were observed in the aqueous and solid phases during reactions.Our study may have important implications for further understanding of As behavior and Fe/S cycling thatmay occur under an anoxic environment more comprehensively.展开更多
Currently,endeavors to scale up the production of amorphous catalysts are still impeded by intricate synthesis conditions.Here,we have prepared a series of metal-based molybdate via one-step coprecipitation method.Aft...Currently,endeavors to scale up the production of amorphous catalysts are still impeded by intricate synthesis conditions.Here,we have prepared a series of metal-based molybdate via one-step coprecipitation method.After ingredient optimization,amorphous Co_(2)CeFe_(2)-MoO_(4) was identified as exhibiting the highest intrinsic activity among its counterparts.Modulation of electron structure enables Co_(2)CeFe_(2)-MoO_(4) to balance the adsorption behavior towards reactive intermediates.Ultimately,the obtained Co_(2)CeFe_(2)-MoO_(4) molybdate demonstrated a captivating OER performance,showcasing a low overpotential of 230 mV at 10 mA cm^(-2).Moreover,the alkaline electrolyzer employing the Co_(2)CeFe_(2)-MoO_(4) anode exhibited a low cell voltage of 1.50 V for water splitting and underwent an acceptable attenuation of 4.99% after 165 h of continuous operation,demonstrating its favorable catalytic activity and durability.This work provides a facile and eco-friendly synthesis pathway for crafting cost-effective and durable earth-abundant OER electrocatalysts tailored for water splitting to produce clean hydrogen.展开更多
La0.72Ca0.28MnO3 thin films were deposited on untilted and 15° tilted LaAlO_3 （100） single crystalline substrates by pulsed laser deposition. The polycrystalline targets used in the deposition process were synt...La0.72Ca0.28MnO3 thin films were deposited on untilted and 15° tilted LaAlO_3 （100） single crystalline substrates by pulsed laser deposition. The polycrystalline targets used in the deposition process were synthesized by sol-gel and coprecipitation methods, respectively. The structure, electrical transport properties and surface morphology of the targets and films were studied. It is found that, compared with coprecipitation method, the sol-gel target has more homogeneous components and larger density and grain size, thus the higher insulator-metal transition temperature and larger temperature coefficient of resistivity. The thin film prepared by sol-gel target has a uniform grain size and higher quality. The metal-insulator transition temperature is higher and the laser induced voltage signal is larger. Preparing the target by sol-gel method can largely improve the properties of corresponding thin films in pulsed laser deposition process.展开更多
Cerium-doped yttrium aluminum garnet（YAG：Ce） as a yellow phosphor for white light-emitting diodes（LEDs） was synthesized via a facile combustion method using Y2 O3, CeO2, Al2 O3, Al,and NaClO4 as raw materials. Th...Cerium-doped yttrium aluminum garnet（YAG：Ce） as a yellow phosphor for white light-emitting diodes（LEDs） was synthesized via a facile combustion method using Y2 O3, CeO2, Al2 O3, Al,and NaClO4 as raw materials. The combustion synthesis approach utilizes the strong exothermic oxidation of aluminum to realize a self-sustaining reaction. In this study, we investigated the effects of the ratios of Al2 O3 to AI,fluxes, and coprecipitated materials as raw materials on the luminescence properties of the synthesized YAG：Ce phosphors. When the amount of Al2 O3 x is varied, the combustion reaction proceeds at x ≤ 1.8,with x = 1.725 being the optimum condition for producing a high-performance product. When 5 wt%BaF2 is added, the luminescence intensity is significantly improved owing to a decrease of YAP（YAlO3）formation with improved uniformity. However, the addition of CaF2 and NaF does not improve the luminescence properties. To suppress the segregation of CeO2, we used the coprecipitated material Y2 O3-CeO2 as a raw material. Unlike with separate addition of Y2 O3 and CeO2, Ce ions are uniformly distributed in the coprecipitated material, resulting in improved luminescence properties. The combination of BaF2 and coprecipitated material significantly improves the internal quantum efficiency to83.0%, which is close to that of commercial phosphors.展开更多
The ultrafine Ce-based oxide nanoparticles with different element dopings （Zr, Y） were synthesized by the method of mi- cropores-diffused coprecipitation （MDC） using ammonia solution as the precipitation agent. Th...The ultrafine Ce-based oxide nanoparticles with different element dopings （Zr, Y） were synthesized by the method of mi- cropores-diffused coprecipitation （MDC） using ammonia solution as the precipitation agent. The activities of the catalysts for soot oxidation were evaluated by the temperature-programmed oxidation （TPO） reaction. Ce-based oxides prepared in this study exhibited high catalytic activity for soot oxidation under tile condition of loose contact between soot particles and catalysts, and the catalytic ac- tivity ofultrafine Ce0.gZr0 iO2 nanoparticle for soot combustion was the highest, whose/＂10, Ts0 and Sco2m was 364, 442 ~C and 98.3%, respectively. All catalysts were systematically characterized by means of X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Brumauer-Emett-Teller （BET）, Fourier transform infrared spectroscopy （FT-IR） and UV-Vis diffuse reflectance spectroscopy （UV-Vis DRS）. It was indicated that the MDC method could prepare the ultrafine Ce-bascd oxide nanoparticles whose the crystal lattice were perfect, and the BET surface area and average crystal size of the ultrafine nanoparticles changed with the different element dopings （Zr, Y）. The H2-TPR measurements showed that the ultrafine Ce-based ox- ide nanoparticles with the doping-Zr cation could be favorable for improving the redox property of the catalysts.展开更多
A uniform Al-doped LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2) cathode material was prepared using a coprecipitation method to take advantage of the positive effect of Al on regenerated NCM(Ni,Co,Mn)cathode materials and ameliora...A uniform Al-doped LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2) cathode material was prepared using a coprecipitation method to take advantage of the positive effect of Al on regenerated NCM(Ni,Co,Mn)cathode materials and ameliorate cumbersome and high-cost impurity removal processes during lithium-ion battery recycling.When the Al^(3+) content in the leachate was 1 at.%with respect to the total amount of transition metals(Ni,Co,and Mn),the produced Al-doped NCM cathode material increased concentrations of lattice oxygen and Ni^(2+).The initial specific capacity at 0.1C was 167.4 mA·h/g,with a capacity retention of 79.1%after 400 cycles at 1C.Further,this Al-doped sample showed improved rate performance and a smaller electrochemical impedance.These findings provide a reference for developing industrial processes to resynthesize cathode materials with improved electrochemical performance by incorporating Al^(3+) impurities produced during lithium-ion battery recycling.展开更多
Indium tin oxide （ITO） nanoparticles with crystallite size of 12.6 nm and specific surface area of 45.7 m 2 ·g-1 were synthesized by co-precipitation method.The indium solution was obtained by dissolving metal ...Indium tin oxide （ITO） nanoparticles with crystallite size of 12.6 nm and specific surface area of 45.7 m 2 ·g-1 were synthesized by co-precipitation method.The indium solution was obtained by dissolving metal indium in HNO3.The tin solution was obtained by dissolving metal tin in HNO3 and followed by stabilizing with citric acid.The free of chlorine ions in the synthesis process brought several advantages：shortening the synthesis time,decreasing the particle agglomeration,decreasing the chlorine content in the ITO nanoparticles and improving the particle sinterability.This is the first time to report the synthesis of ITO nanoparticles free from chlorine contamination without using the expensive metal alkoxides as starting materials.展开更多
The new Cu-Co based （Cu/Co/Zn/Zr） catalysts for higher-alcohol synthesis were prepared using coprecipitation method, plasma enhanced method and reverse coprecipitation method under ultrasound irradiation. The cataly...The new Cu-Co based （Cu/Co/Zn/Zr） catalysts for higher-alcohol synthesis were prepared using coprecipitation method, plasma enhanced method and reverse coprecipitation method under ultrasound irradiation. The catalysts were investigated by the means of BET, SEM, XRD, H2-TPR and XPS. Catalytic properties of the catalysts prepared by various methods were examined using CO hydrogenation reaction. It was found that plasma enhanced method and reverse coprecipitation method under ultrasound irradiation were both effective in enhancing the catalytic properties of Cu/Co/Zn/Zr mixed oxides. The small particle size, high dispersion of active components, the improvement of specific surface area and surface contents of active phases could account for the excellent performance of the experimental Cu/Co/Zn/Zr catalysts.展开更多
In order to improve the electrochemical performance and thermal stability of Li1.05Co1/3Nil/3Mnl/302 materials, Lil.05CO0.3 Ni0.35Mno.3Mo.0502（M=Ge,Sn） cathode materials were synthesized via co-precipitation method....In order to improve the electrochemical performance and thermal stability of Li1.05Co1/3Nil/3Mnl/302 materials, Lil.05CO0.3 Ni0.35Mno.3Mo.0502（M=Ge,Sn） cathode materials were synthesized via co-precipitation method. The structure, electrochemical performance and thermal stability were characterized by X-ray diffraction（XRD）, charge/discharge cycling, cyclic voltammetry（CV）, electrochemical impedance spectroscopy（EIS） and differential scanning calorimetry（DSC）. ESEM showed that Sn-doped and Ge- doped slightly increased the size of grains. XRD and CV showed that Sn-doped and Ge-doped powders were homogeneous and had the better layered structure than the bare one. Sn-doped and Ge-doped improved high rate discharge capacity and cycle-life performance. The reason of the better cycling performance of the doped one was the increasing of lithium-ion diffusion rate and charge transfer rate. Sn-doped and Ge-doped also improved the mateials thermal stability.展开更多
Ceria-zirconia based mixed oxides(CZs)have been applied in three-way catalysts(TWCs)for their high surface area and oxygen storage capacity(OSC).In this work,enhanced thermal stability of Ce_(0.33)Zr_(0.55)(LaNdY)_(0....Ceria-zirconia based mixed oxides(CZs)have been applied in three-way catalysts(TWCs)for their high surface area and oxygen storage capacity(OSC).In this work,enhanced thermal stability of Ce_(0.33)Zr_(0.55)(LaNdY)_(0.12)O_(2)mixed oxides was realized via a facile and scalable approach,namely,sulfateaided coprecipitation method was labelled as CZ-S.Sulfate ion(SO_(4)^(2-))was added into raw solution in the form of sulfuric acid and acted as coordination agent.The control sample was prepared by conventional coprecipitation method without sulfuric acid added and labelled as CZ.The promotion effect of sulfate ion was analyzed systematically by X-ray diffraction(XRD),transmission electron microscopy(TEM),scanning electron microscopy(SEM),N_(2)adsorption-desorption,Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),OSC and hydrogen temperatureprogrammed reduction(H_(2)-TPR)analysis.XRD and high resolution TEM results reveal that CZ-S have homogeneous distributions of elements.TEM and SEM images show that fresh samples of CZ-S have narrower distributions of grain sizes and larger pore sizes than those of CZ.Through cross analysis of structure and morphology of CZ and CZ-S,we find that the introduction of sulfate ions results in uniform distributions of elements,narrows distributions of grain sizes,and enables the formation of secondary loose packing of sub-particles,which lead to enhanced thermal stability of the samples of CZ-S upon aging process at high temperature.After aging treatment at 1100℃for 10 h,aged samples of CZ-S present larger specific surface areas and pore volumes than the aged sample prepared by conventional coprecipitation method without sulfate ions added.Furthermore,the aged sample of CZ-S2(SO_(4)^(2-)/Zr=1)possesses the highest specific surface area of 21.9 m2/g and the biggest pore volume of 0.035 mL/g among all aged samples.展开更多
The nanopowders of Mg-Al carbonate layered double hydroxides （MgAl-LDH） were prepared via coprecipitation process. ZnO nanoparticles were homogeneously coated on the ceramic MgAl-LDH surface. After calcination at 50...The nanopowders of Mg-Al carbonate layered double hydroxides （MgAl-LDH） were prepared via coprecipitation process. ZnO nanoparticles were homogeneously coated on the ceramic MgAl-LDH surface. After calcination at 500℃ for 4 h, X-ray diffraction and scanning electron microscopy were employed to investigate the crystal structure and morphology, respectively. It was demonstrated that ZnO nanoparticles were successfully prepared on ceramic MgAI-LDH support. The obtained nano-ZnO photocatalyst showed a high photocatalytic degradation of malachite green. The enhanced photocatalytic property can be attributed to both high photocatalytic activity of ZnO and good adsorption behavior of ceramic MgAI-LDH, in which the flaky structure of MgAI-LDH plays an important role.展开更多
Dry reforming of methane by CO2 using nickel ferrite as precursor of catalysts was investigated.Nickel ferrite crystalline particles were prepared by coprecipitation of nitrates with NaOH or ammonia followed by calcin...Dry reforming of methane by CO2 using nickel ferrite as precursor of catalysts was investigated.Nickel ferrite crystalline particles were prepared by coprecipitation of nitrates with NaOH or ammonia followed by calcination,or by hydrothermal synthesis without calcination step.The textural and structural properties were determined by a number of analysis methods,including X-ray diffraction （XRD）,Raman spectroscopy and X-ray photoelectron spectroscopy （XPS）,among which X-ray diffraction （XRD） was at room and variable temperatures.All synthesized oxides showed the presence of micro or nanoparticles of NiFe2O4 inverse spinel,but Fe2O3 （hematite） was also present when ammonia was used for coprecipitation.The reducibility by hydrogen was studied by temperature-programmed reduction （TPR） and in situ XRD,which showed the influence of the preparation method.The surface area （BET）,particle size （Rietveld refinement）,as well as surface Ni/Fe atomic ratio （XPS） and the behavior upon reduction varied according to the synthesis method.The catalytic reactivity was investigated using isopropanol decomposition to determine the acid/base properties.The catalytic performance of methane reforming with CO2 was measured with and without the pre-treatment of catalysts under H2 in 650-800 C range.The catalytic conversions of methane and CO2 were quite low but they increased when the catalysts were pre-reduced.A significant contribution of reverse water gas shift reaction accounted for the low values of H2 /CO ratio.No coking was observed as shown by the reoxidation step performed after the catalytic reactions.The possible formation of nickel-iron alloy observed during the study of reducibility by hydrogen was invoked to account for the catalytic behavior.展开更多
Photocatalytic H2evolution under visible light irradiation is an ideal process for solving energy shortage.The low cost of photocatalysts and high efficiency of hydrogen evolution are the two key factors to realize th...Photocatalytic H2evolution under visible light irradiation is an ideal process for solving energy shortage.The low cost of photocatalysts and high efficiency of hydrogen evolution are the two key factors to realize the industrialization of the process.The substitution of a noble‐metal cocatalyst with a non‐noble‐metal catalyst can significantly reduce the cost of the photocatalyst.The largescale synthesis and assembly of semiconductors and non‐noble‐metal cocatalysts to form photocatalysts through a simple method can further decrease the cost of photocatalysis.Here,we report a large‐scale and low‐cost coprecipitation method to form phosphide/CdS photocatalysts to realize photocatalytic H2evolution.CoP and MoP cocatalysts significantly enhanced the photocatalytic production of hydrogen.The optimal H2production rates on CoP/CdS and MoP/CdS were140and78μmol/h,which were7.0and4.0times higher than those obtained with bare CdS,respectively,and2.0times and1.1times higher than those obtained with1.0%Pt/CdS,respectively.This work provides a practical method for the large‐scale preparation of low‐cost photocatalysts.展开更多
Ceria-zirconia(CZ)and ceria-terbia(CT)and alumina-supported ceria-zirconia(CZA)and ceria-terbia(CTA)solid solutions were synthesized by coprecipitation and deposition precipitation methods,respectively.Structural char...Ceria-zirconia(CZ)and ceria-terbia(CT)and alumina-supported ceria-zirconia(CZA)and ceria-terbia(CTA)solid solutions were synthesized by coprecipitation and deposition precipitation methods,respectively.Structural characteristics and catalytic activity of the synthesized samples have been investigated using X-ray diffraction(XRD),high resolution transmission electron microscopy(HRTEM),X-ray photoelectron spectroscopy(XPS),Raman spectroscopy(RS),and Brunauer-Emmett-Teller(BET)surface area measurements.To evaluate the catalytic properties,total oxygen storage capacity and CO oxidation activity measurements were carried out.The XRD analyses revealed the formation of Ce0.75Zr0.25O2 phase for CZ and Ce0.5Zr0.5O2 and Ce0.6Zr0.4O2 phases for CZA samples,respectively.While the formation of only Ce0.8Tb0.2O2-δphase was noted for both CT and CTA samples.All the supported and unsupported samples adopted a fluorite-type structure and exhibited cell parameters with respect to Vegard's rule.The HRTEM results indicated well-dispersed particles of the size around 5 nm.The RS measurements suggested the presence of oxygen vacancies due to defective structure formation.The XPS studies revealed the presence of cerium in both Ce 4+ and Ce 3+ oxidation states in different proportions.It was found that CO oxidation for CTA occurs at very much lower temperature than CT,CZ,and CZA samples.Details of these findings by correlating with the structural characterization studies are consolidated.展开更多
The La-modified Cu-Mn spinel oxide was successfully coated onto honeycomb ceramic by a washcoating method for complete catalytic decomposition of ethyl acetate.The La-modified Cu-Mn oxides were characterized by X-ray ...The La-modified Cu-Mn spinel oxide was successfully coated onto honeycomb ceramic by a washcoating method for complete catalytic decomposition of ethyl acetate.The La-modified Cu-Mn oxides were characterized by X-ray diffraction,X-ray fluorescence,H_(2)-temperature programmed reduction,Brunauer-Emmett-Teller method,field-emission scanning electron microscopy and high-resolution transmission electron microscopy.The effects of different precipitants and rare earth doping on the structure and catalytic performance of the catalysts were investigated.The results show that the CuMn_(2)O_(4) spinel with(NH_(4))_(2)CO_(3) as a precipitant can form a larger specific surface area and a suitable pore size,which is beneficial to the absorption of ethyl acetate.Although the rare earth doping does not significantly change the crystal phase structure of the catalyst,it improves its reducibility and lowers the temperature of the catalytic decomposition.With respect to the catalytic decomposition of ethyl acetate,the rare earth-modified Cu-Mn oxide supported on honeycomb ceramic shows excellent catalytic performance with 100% conversion under the conditions of 239℃,space velocity of 12500 h^(-1) and 1000 ppm.And the ethyl acetate removal rate is still 100% after 1440 min of continuous reaction.展开更多
Rare earth ion （Nd^3＋/Y^3＋） and Al^3＋ codoped α-Ni（OH）2 powers were synthesized by chemical coprecipitation method. The structttre was analyzed with X-ray diffraction （XRD） and thermal gravity （TG）. Cyclic...Rare earth ion （Nd^3＋/Y^3＋） and Al^3＋ codoped α-Ni（OH）2 powers were synthesized by chemical coprecipitation method. The structttre was analyzed with X-ray diffraction （XRD） and thermal gravity （TG）. Cyclic voltammetry （CV） tests were performed to evaluate the proton diffusion coefficients of the samples. The results indicated that codoping of Y-Al and Nd-Al resulted in more water molecules contained within the crystal lattice and accordingly increased the interlayer spacing. In particular, the Y-Al codoped α-Ni（OH）2 showed a turbostratic structure. The calculated diffusion coefficients of the Y-Al codoped α-Ni（OH）2 and Nd-Al codoped α-Ni（OH）2 were 3.5×10^-10cm^2/s and 2.8× 10^-10 cm^2/s, respectively.展开更多
Aluminum-doped zinc oxide （ZnO：Al）, abbreviated as ZAO, is a novel and widely used transparent conductive material. The ZAO powder was synthesized by chemical coprecipitation. The ZAO ceramic sputtering target mate...Aluminum-doped zinc oxide （ZnO：Al）, abbreviated as ZAO, is a novel and widely used transparent conductive material. The ZAO powder was synthesized by chemical coprecipitation. The ZAO ceramic sputtering target materials were fabricated by sintering in air, and ZAO transparent conductive films were prepared by RF magnetron sputtering on glass substrates. XRD proved that such films had an orientation of （002） crystal panel paralleled to the surface of the glass substrate. The average transmittance of the films in the visible region exceeded 80%.展开更多
The objective of this study was to establish the dielectric properties of CoFe2O4 nanoparticles with particle sizes that varied from 28.6 to 5.8 nm. CoFe2O4 nanoparticles were synthesized using a chemical coprecipitat...The objective of this study was to establish the dielectric properties of CoFe2O4 nanoparticles with particle sizes that varied from 28.6 to 5.8 nm. CoFe2O4 nanoparticles were synthesized using a chemical coprecipitation method. The particle sizes were calculated accord-ing to the Scherrer formula using X-ray diffraction （XRD） peaks, and the particle size distribution curves were constructed by using field-emission scanning electron microscopy （FESEM） images. The dielectric permittivity and loss tangents of the samples were determined in the frequency range of 1 kHz to 1 MHz and in the temperature range of 300 to 10 K. Both the dielectric permittivity and the loss tangent were found to decrease with increasing frequency and decreasing temperature. For the smallest CoFe2O4 nanoparticle size, the dielectric per-mittivity and loss tangent exhibited their highest and lowest values, respectively. This behavior is very useful for materials used in devices that operate in the microwave or radio frequency ranges.展开更多
文摘Silver-ceramics (Ag2MO2)(M=Co, Ni, or Cu) were prepared through thermal decompositionof coprecipitated oxalates. Pellets of these materials were annealed at 350℃ for different timeperiods up to 5 h. The effect of annealing time on the transport properties was studied. IR andX-ray spectra were also studied.
基金The authors thank Prof. Yi-lu Fu and Prof. Peiyan Lin for their kind help. This work was supported by the 863 Program （No.2006AA05Z118）, 973 Program （No.2007CB210206）, and the National Natural Science Foundation of China （No.50772107）.
文摘The effects of potassium addition and the potassium content on the activity and selectivity of coprecipitated iron catalyst for Fischer-Tropsch synthesis （FTS） were studied in a fixed bed reactor at 1.5 MPa, 300 ℃, and contact time （W/F） of 12.5 gcath/mol using the model bio-oil-syngas of H2/CO/CO2/N2 （62/8/25/5, vol%）. It was found that potassium addition increases the catalyst activity for FTS and the reverse water gas shift reaction. Moreover, potassium increases the average molecular weight （chain length） of the hydrocarbon products. With the increase of potassium content, it was found that CH4 selectivity decreases and the selectivity of liquid phase products （C5＋） increases. The characteristics of FTS catalysts with different potassium content were also investigated by various characterization measurements including X-ray diffraction, X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller surface area. Based on experimental results, 100Fe/6Cu/16Al/6K （weight ratio） was selected as the optimal catalyst for FTS from bio-oil-syngas. The results indicate that the 100Fe/6Cu/16Al/6K catalyst is one of the most promising candidates to directly synthesize liquid bio-fuel using bio-oil-syngas.
基金supported by the National Key Research and Development Program of China(No.2022YFC3701301)the National Natural Science Foundation of China(Nos.42173063 and 42377251)+1 种基金the Youth Innovation Promotion Association CAS(No.2020200)the Fundamental Research Funds for the Central Universities.
文摘In sulfidic anoxic environments,iron sulfides are widespread solid phases that play an important role in the arsenic(As)biogeochemical cycle.This work investigated the transformation process of FeS-As coprecipitates,the concurrent behavior,and the speciation of associated As under anoxic conditions.The results showed that FeS-As coprecipitates could convert to greigite and pyrite.The transformation degree of the produced solid phases was dependent upon the pH conditions and initial As species.These results showed that the As mobilization was closely associated with the solid phase transformation.The solid phase transformationwent from disordered mackinawite to crystallinemackinawite,then greigite and finally pyrite.The As in the coprecipitates underwent a process of release,fixation,and release again.Both reduction of As(Ⅴ)and oxidation of As(Ⅲ)were observed in the aqueous and solid phases during reactions.Our study may have important implications for further understanding of As behavior and Fe/S cycling thatmay occur under an anoxic environment more comprehensively.
基金supported by the National Natural Science Foundation of China (No. 21872153)。
文摘Currently,endeavors to scale up the production of amorphous catalysts are still impeded by intricate synthesis conditions.Here,we have prepared a series of metal-based molybdate via one-step coprecipitation method.After ingredient optimization,amorphous Co_(2)CeFe_(2)-MoO_(4) was identified as exhibiting the highest intrinsic activity among its counterparts.Modulation of electron structure enables Co_(2)CeFe_(2)-MoO_(4) to balance the adsorption behavior towards reactive intermediates.Ultimately,the obtained Co_(2)CeFe_(2)-MoO_(4) molybdate demonstrated a captivating OER performance,showcasing a low overpotential of 230 mV at 10 mA cm^(-2).Moreover,the alkaline electrolyzer employing the Co_(2)CeFe_(2)-MoO_(4) anode exhibited a low cell voltage of 1.50 V for water splitting and underwent an acceptable attenuation of 4.99% after 165 h of continuous operation,demonstrating its favorable catalytic activity and durability.This work provides a facile and eco-friendly synthesis pathway for crafting cost-effective and durable earth-abundant OER electrocatalysts tailored for water splitting to produce clean hydrogen.
基金Project(50902062)supported by the National Natural Science Foundation of ChinaProject(KKZ1200927002)supported by Key Programme of Kunming University of Science and Technology,China
文摘La0.72Ca0.28MnO3 thin films were deposited on untilted and 15° tilted LaAlO_3 （100） single crystalline substrates by pulsed laser deposition. The polycrystalline targets used in the deposition process were synthesized by sol-gel and coprecipitation methods, respectively. The structure, electrical transport properties and surface morphology of the targets and films were studied. It is found that, compared with coprecipitation method, the sol-gel target has more homogeneous components and larger density and grain size, thus the higher insulator-metal transition temperature and larger temperature coefficient of resistivity. The thin film prepared by sol-gel target has a uniform grain size and higher quality. The metal-insulator transition temperature is higher and the laser induced voltage signal is larger. Preparing the target by sol-gel method can largely improve the properties of corresponding thin films in pulsed laser deposition process.
基金supported by the"Nanotechnology Platform"Program of the Ministry of Education,Culture,Sports,Science and Technology of Japan(MEXT)
文摘Cerium-doped yttrium aluminum garnet（YAG：Ce） as a yellow phosphor for white light-emitting diodes（LEDs） was synthesized via a facile combustion method using Y2 O3, CeO2, Al2 O3, Al,and NaClO4 as raw materials. The combustion synthesis approach utilizes the strong exothermic oxidation of aluminum to realize a self-sustaining reaction. In this study, we investigated the effects of the ratios of Al2 O3 to AI,fluxes, and coprecipitated materials as raw materials on the luminescence properties of the synthesized YAG：Ce phosphors. When the amount of Al2 O3 x is varied, the combustion reaction proceeds at x ≤ 1.8,with x = 1.725 being the optimum condition for producing a high-performance product. When 5 wt%BaF2 is added, the luminescence intensity is significantly improved owing to a decrease of YAP（YAlO3）formation with improved uniformity. However, the addition of CaF2 and NaF does not improve the luminescence properties. To suppress the segregation of CeO2, we used the coprecipitated material Y2 O3-CeO2 as a raw material. Unlike with separate addition of Y2 O3 and CeO2, Ce ions are uniformly distributed in the coprecipitated material, resulting in improved luminescence properties. The combination of BaF2 and coprecipitated material significantly improves the internal quantum efficiency to83.0%, which is close to that of commercial phosphors.
基金supported by National Natural Science Foundation of China(21177160,21173270 and 21303263)
文摘The ultrafine Ce-based oxide nanoparticles with different element dopings （Zr, Y） were synthesized by the method of mi- cropores-diffused coprecipitation （MDC） using ammonia solution as the precipitation agent. The activities of the catalysts for soot oxidation were evaluated by the temperature-programmed oxidation （TPO） reaction. Ce-based oxides prepared in this study exhibited high catalytic activity for soot oxidation under tile condition of loose contact between soot particles and catalysts, and the catalytic ac- tivity ofultrafine Ce0.gZr0 iO2 nanoparticle for soot combustion was the highest, whose/＂10, Ts0 and Sco2m was 364, 442 ~C and 98.3%, respectively. All catalysts were systematically characterized by means of X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Brumauer-Emett-Teller （BET）, Fourier transform infrared spectroscopy （FT-IR） and UV-Vis diffuse reflectance spectroscopy （UV-Vis DRS）. It was indicated that the MDC method could prepare the ultrafine Ce-bascd oxide nanoparticles whose the crystal lattice were perfect, and the BET surface area and average crystal size of the ultrafine nanoparticles changed with the different element dopings （Zr, Y）. The H2-TPR measurements showed that the ultrafine Ce-based ox- ide nanoparticles with the doping-Zr cation could be favorable for improving the redox property of the catalysts.
基金supported by Anhui Province Research and Development Innovation Project for Automotive Power Battery Efficient Recycling System, China
文摘A uniform Al-doped LiNi_(0.5)Co_(0.2)Mn_(0.3)O_(2) cathode material was prepared using a coprecipitation method to take advantage of the positive effect of Al on regenerated NCM(Ni,Co,Mn)cathode materials and ameliorate cumbersome and high-cost impurity removal processes during lithium-ion battery recycling.When the Al^(3+) content in the leachate was 1 at.%with respect to the total amount of transition metals(Ni,Co,and Mn),the produced Al-doped NCM cathode material increased concentrations of lattice oxygen and Ni^(2+).The initial specific capacity at 0.1C was 167.4 mA·h/g,with a capacity retention of 79.1%after 400 cycles at 1C.Further,this Al-doped sample showed improved rate performance and a smaller electrochemical impedance.These findings provide a reference for developing industrial processes to resynthesize cathode materials with improved electrochemical performance by incorporating Al^(3+) impurities produced during lithium-ion battery recycling.
基金supported by the Ph.D. programs Foundation of Ministry of Education of China (No.200802511022)
文摘Indium tin oxide （ITO） nanoparticles with crystallite size of 12.6 nm and specific surface area of 45.7 m 2 ·g-1 were synthesized by co-precipitation method.The indium solution was obtained by dissolving metal indium in HNO3.The tin solution was obtained by dissolving metal tin in HNO3 and followed by stabilizing with citric acid.The free of chlorine ions in the synthesis process brought several advantages：shortening the synthesis time,decreasing the particle agglomeration,decreasing the chlorine content in the ITO nanoparticles and improving the particle sinterability.This is the first time to report the synthesis of ITO nanoparticles free from chlorine contamination without using the expensive metal alkoxides as starting materials.
基金supported by the National Natural Science Foundation of China(205903603)the New Century Excellent Talent Project of China(NCET-05-0783)
文摘The new Cu-Co based （Cu/Co/Zn/Zr） catalysts for higher-alcohol synthesis were prepared using coprecipitation method, plasma enhanced method and reverse coprecipitation method under ultrasound irradiation. The catalysts were investigated by the means of BET, SEM, XRD, H2-TPR and XPS. Catalytic properties of the catalysts prepared by various methods were examined using CO hydrogenation reaction. It was found that plasma enhanced method and reverse coprecipitation method under ultrasound irradiation were both effective in enhancing the catalytic properties of Cu/Co/Zn/Zr mixed oxides. The small particle size, high dispersion of active components, the improvement of specific surface area and surface contents of active phases could account for the excellent performance of the experimental Cu/Co/Zn/Zr catalysts.
基金Funded by the Natural Science Fundation of Youth Fund in Hebei Province Universities in 2011(No:2011211)
文摘In order to improve the electrochemical performance and thermal stability of Li1.05Co1/3Nil/3Mnl/302 materials, Lil.05CO0.3 Ni0.35Mno.3Mo.0502（M=Ge,Sn） cathode materials were synthesized via co-precipitation method. The structure, electrochemical performance and thermal stability were characterized by X-ray diffraction（XRD）, charge/discharge cycling, cyclic voltammetry（CV）, electrochemical impedance spectroscopy（EIS） and differential scanning calorimetry（DSC）. ESEM showed that Sn-doped and Ge- doped slightly increased the size of grains. XRD and CV showed that Sn-doped and Ge-doped powders were homogeneous and had the better layered structure than the bare one. Sn-doped and Ge-doped improved high rate discharge capacity and cycle-life performance. The reason of the better cycling performance of the doped one was the increasing of lithium-ion diffusion rate and charge transfer rate. Sn-doped and Ge-doped also improved the mateials thermal stability.
基金Project supported by Beijing Nova Program(Z181100006218030)。
文摘Ceria-zirconia based mixed oxides(CZs)have been applied in three-way catalysts(TWCs)for their high surface area and oxygen storage capacity(OSC).In this work,enhanced thermal stability of Ce_(0.33)Zr_(0.55)(LaNdY)_(0.12)O_(2)mixed oxides was realized via a facile and scalable approach,namely,sulfateaided coprecipitation method was labelled as CZ-S.Sulfate ion(SO_(4)^(2-))was added into raw solution in the form of sulfuric acid and acted as coordination agent.The control sample was prepared by conventional coprecipitation method without sulfuric acid added and labelled as CZ.The promotion effect of sulfate ion was analyzed systematically by X-ray diffraction(XRD),transmission electron microscopy(TEM),scanning electron microscopy(SEM),N_(2)adsorption-desorption,Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),OSC and hydrogen temperatureprogrammed reduction(H_(2)-TPR)analysis.XRD and high resolution TEM results reveal that CZ-S have homogeneous distributions of elements.TEM and SEM images show that fresh samples of CZ-S have narrower distributions of grain sizes and larger pore sizes than those of CZ.Through cross analysis of structure and morphology of CZ and CZ-S,we find that the introduction of sulfate ions results in uniform distributions of elements,narrows distributions of grain sizes,and enables the formation of secondary loose packing of sub-particles,which lead to enhanced thermal stability of the samples of CZ-S upon aging process at high temperature.After aging treatment at 1100℃for 10 h,aged samples of CZ-S present larger specific surface areas and pore volumes than the aged sample prepared by conventional coprecipitation method without sulfate ions added.Furthermore,the aged sample of CZ-S2(SO_(4)^(2-)/Zr=1)possesses the highest specific surface area of 21.9 m2/g and the biggest pore volume of 0.035 mL/g among all aged samples.
文摘The nanopowders of Mg-Al carbonate layered double hydroxides （MgAl-LDH） were prepared via coprecipitation process. ZnO nanoparticles were homogeneously coated on the ceramic MgAl-LDH surface. After calcination at 500℃ for 4 h, X-ray diffraction and scanning electron microscopy were employed to investigate the crystal structure and morphology, respectively. It was demonstrated that ZnO nanoparticles were successfully prepared on ceramic MgAI-LDH support. The obtained nano-ZnO photocatalyst showed a high photocatalytic degradation of malachite green. The enhanced photocatalytic property can be attributed to both high photocatalytic activity of ZnO and good adsorption behavior of ceramic MgAI-LDH, in which the flaky structure of MgAI-LDH plays an important role.
文摘Dry reforming of methane by CO2 using nickel ferrite as precursor of catalysts was investigated.Nickel ferrite crystalline particles were prepared by coprecipitation of nitrates with NaOH or ammonia followed by calcination,or by hydrothermal synthesis without calcination step.The textural and structural properties were determined by a number of analysis methods,including X-ray diffraction （XRD）,Raman spectroscopy and X-ray photoelectron spectroscopy （XPS）,among which X-ray diffraction （XRD） was at room and variable temperatures.All synthesized oxides showed the presence of micro or nanoparticles of NiFe2O4 inverse spinel,but Fe2O3 （hematite） was also present when ammonia was used for coprecipitation.The reducibility by hydrogen was studied by temperature-programmed reduction （TPR） and in situ XRD,which showed the influence of the preparation method.The surface area （BET）,particle size （Rietveld refinement）,as well as surface Ni/Fe atomic ratio （XPS） and the behavior upon reduction varied according to the synthesis method.The catalytic reactivity was investigated using isopropanol decomposition to determine the acid/base properties.The catalytic performance of methane reforming with CO2 was measured with and without the pre-treatment of catalysts under H2 in 650-800 C range.The catalytic conversions of methane and CO2 were quite low but they increased when the catalysts were pre-reduced.A significant contribution of reverse water gas shift reaction accounted for the low values of H2 /CO ratio.No coking was observed as shown by the reoxidation step performed after the catalytic reactions.The possible formation of nickel-iron alloy observed during the study of reducibility by hydrogen was invoked to account for the catalytic behavior.
基金supported by the National First-rate Discipline Construction Project of Ningxia (Chemical Engineering and Technology)the Major Innovation Projects for Building First-class Universities in China’s Western Region (ZKZD2017003)+2 种基金the University Research Project of Ningxia (NGY2015027)the National Natural Science Foundation of China (21263018)the Project of Science and Technology of Personnel of Study Abroad (Ningxia (2014) 486)~~
文摘Photocatalytic H2evolution under visible light irradiation is an ideal process for solving energy shortage.The low cost of photocatalysts and high efficiency of hydrogen evolution are the two key factors to realize the industrialization of the process.The substitution of a noble‐metal cocatalyst with a non‐noble‐metal catalyst can significantly reduce the cost of the photocatalyst.The largescale synthesis and assembly of semiconductors and non‐noble‐metal cocatalysts to form photocatalysts through a simple method can further decrease the cost of photocatalysis.Here,we report a large‐scale and low‐cost coprecipitation method to form phosphide/CdS photocatalysts to realize photocatalytic H2evolution.CoP and MoP cocatalysts significantly enhanced the photocatalytic production of hydrogen.The optimal H2production rates on CoP/CdS and MoP/CdS were140and78μmol/h,which were7.0and4.0times higher than those obtained with bare CdS,respectively,and2.0times and1.1times higher than those obtained with1.0%Pt/CdS,respectively.This work provides a practical method for the large‐scale preparation of low‐cost photocatalysts.
基金supported by Council of Scientific and Industrial Research(CSIR),New Delhi,India
文摘Ceria-zirconia(CZ)and ceria-terbia(CT)and alumina-supported ceria-zirconia(CZA)and ceria-terbia(CTA)solid solutions were synthesized by coprecipitation and deposition precipitation methods,respectively.Structural characteristics and catalytic activity of the synthesized samples have been investigated using X-ray diffraction(XRD),high resolution transmission electron microscopy(HRTEM),X-ray photoelectron spectroscopy(XPS),Raman spectroscopy(RS),and Brunauer-Emmett-Teller(BET)surface area measurements.To evaluate the catalytic properties,total oxygen storage capacity and CO oxidation activity measurements were carried out.The XRD analyses revealed the formation of Ce0.75Zr0.25O2 phase for CZ and Ce0.5Zr0.5O2 and Ce0.6Zr0.4O2 phases for CZA samples,respectively.While the formation of only Ce0.8Tb0.2O2-δphase was noted for both CT and CTA samples.All the supported and unsupported samples adopted a fluorite-type structure and exhibited cell parameters with respect to Vegard's rule.The HRTEM results indicated well-dispersed particles of the size around 5 nm.The RS measurements suggested the presence of oxygen vacancies due to defective structure formation.The XPS studies revealed the presence of cerium in both Ce 4+ and Ce 3+ oxidation states in different proportions.It was found that CO oxidation for CTA occurs at very much lower temperature than CT,CZ,and CZA samples.Details of these findings by correlating with the structural characterization studies are consolidated.
基金Project supported by Chongqing Science and Technology Bureau(cstc2018jscx-msybX0057,cstc2020j scx-msxm038)Chongqing Science and Technology Bureau Key Research and Development Project(cstc2018jszxzdyfxmX0018)。
文摘The La-modified Cu-Mn spinel oxide was successfully coated onto honeycomb ceramic by a washcoating method for complete catalytic decomposition of ethyl acetate.The La-modified Cu-Mn oxides were characterized by X-ray diffraction,X-ray fluorescence,H_(2)-temperature programmed reduction,Brunauer-Emmett-Teller method,field-emission scanning electron microscopy and high-resolution transmission electron microscopy.The effects of different precipitants and rare earth doping on the structure and catalytic performance of the catalysts were investigated.The results show that the CuMn_(2)O_(4) spinel with(NH_(4))_(2)CO_(3) as a precipitant can form a larger specific surface area and a suitable pore size,which is beneficial to the absorption of ethyl acetate.Although the rare earth doping does not significantly change the crystal phase structure of the catalyst,it improves its reducibility and lowers the temperature of the catalytic decomposition.With respect to the catalytic decomposition of ethyl acetate,the rare earth-modified Cu-Mn oxide supported on honeycomb ceramic shows excellent catalytic performance with 100% conversion under the conditions of 239℃,space velocity of 12500 h^(-1) and 1000 ppm.And the ethyl acetate removal rate is still 100% after 1440 min of continuous reaction.
基金the Guangxi Science Research and Technology Developing Foundation (0731001)
文摘Rare earth ion （Nd^3＋/Y^3＋） and Al^3＋ codoped α-Ni（OH）2 powers were synthesized by chemical coprecipitation method. The structttre was analyzed with X-ray diffraction （XRD） and thermal gravity （TG）. Cyclic voltammetry （CV） tests were performed to evaluate the proton diffusion coefficients of the samples. The results indicated that codoping of Y-Al and Nd-Al resulted in more water molecules contained within the crystal lattice and accordingly increased the interlayer spacing. In particular, the Y-Al codoped α-Ni（OH）2 showed a turbostratic structure. The calculated diffusion coefficients of the Y-Al codoped α-Ni（OH）2 and Nd-Al codoped α-Ni（OH）2 were 3.5×10^-10cm^2/s and 2.8× 10^-10 cm^2/s, respectively.
文摘Aluminum-doped zinc oxide （ZnO：Al）, abbreviated as ZAO, is a novel and widely used transparent conductive material. The ZAO powder was synthesized by chemical coprecipitation. The ZAO ceramic sputtering target materials were fabricated by sintering in air, and ZAO transparent conductive films were prepared by RF magnetron sputtering on glass substrates. XRD proved that such films had an orientation of （002） crystal panel paralleled to the surface of the glass substrate. The average transmittance of the films in the visible region exceeded 80%.
文摘The objective of this study was to establish the dielectric properties of CoFe2O4 nanoparticles with particle sizes that varied from 28.6 to 5.8 nm. CoFe2O4 nanoparticles were synthesized using a chemical coprecipitation method. The particle sizes were calculated accord-ing to the Scherrer formula using X-ray diffraction （XRD） peaks, and the particle size distribution curves were constructed by using field-emission scanning electron microscopy （FESEM） images. The dielectric permittivity and loss tangents of the samples were determined in the frequency range of 1 kHz to 1 MHz and in the temperature range of 300 to 10 K. Both the dielectric permittivity and the loss tangent were found to decrease with increasing frequency and decreasing temperature. For the smallest CoFe2O4 nanoparticle size, the dielectric per-mittivity and loss tangent exhibited their highest and lowest values, respectively. This behavior is very useful for materials used in devices that operate in the microwave or radio frequency ranges.
