The KxNa1-xNbO3 nanopowders with cubic-like morphology and an average size of about 50 nm were synthesized by sol-gel auto-combustion method.And then,the ceramics were prepared and the phase transition,microstructure ...The KxNa1-xNbO3 nanopowders with cubic-like morphology and an average size of about 50 nm were synthesized by sol-gel auto-combustion method.And then,the ceramics were prepared and the phase transition,microstructure and electrical properties of the KxNa1-xNbO3 ceramics were investigated.Pure perovskite phases of the KxNa1-xNbO3 ceramics were confirmed by XRD patterns and the K0.50Na0.50NbO3 ceramics show the coexistence of orthorhombic and monoclinic structures.SEM micrographs show that all samples have bimodal grain size distributions and the number of the small grains decrease with increasing K+content in the bimodal grain size distribution system.The K0.50Na0.50NbO3 ceramics with the uniform grain size and the maximum density show excellent electrical properties withεr=467.40,tanδ=0.020,d33=128 pC/N and kp=0.32 at the room temperature,demonstrating that the properties of the K0.50Na0.50NbO3 powers prepared by sol-gel auto-combustion are excellent and the ceramics are promising lead-free piezoelectric materials.展开更多
Calcium looping method has been considered as one of the efficient options to capture C02 in the combustion Ilue gas. CaO-based sorbent is the basis for application of calcium looping and should be subjected to the se...Calcium looping method has been considered as one of the efficient options to capture C02 in the combustion Ilue gas. CaO-based sorbent is the basis for application of calcium looping and should be subjected to the severe calcination condition so as to obtain the concentrated C02 stream. In this research, CaO/CaZrO3 sorbents were synthesized using the sol-gel combustion synthesis （SGCS） method with urea as fuel. The cyclic reaction performance of the synthesized sorbents was evaluated on a lab-scaled reactor system through calcination at 950 ℃ in a pure C02 atmosphere and carbonation at 650 ℃ in the 15% （by volume） C02. The mass ratio of CaO to CaZr03 as 8：2 （designated as CasZr2） was screened as the best option among all the synthesized CaO sorbents for its high CO2 capture capacity and carbonation conversion at the initial cycle. And then a gradual decay in the C02 capture capacity was observed at the following 10 successive cycles, but hereafter stabilized throughout the later cycles. Furthermore, structural evolution of the carbonated CasZr2 over the looping cycles was investigated. With increasing looping cycles, the pore peak and mean grain size of the carbonated CasZr2 sorbent shifted to the bigger direction but both the surface area （SA） ratio and surface fractal dimension Ds decreased. Finally, morphological transformation of the carbonated CasZr2 was observed. Agglomeration and edge rounding of the newly formed CaC03 grains were found as aggravated at the cyclic carbonation stage. As a result, carbonation of CasZr2 with C02 was observed only confined to the external active CaO by the fast formation of the CaC03 shell outside, which occluded the further carbonation of the unreacted CaO inside. Therefore, enough attention should be paid to the carbonation stage and more effective activation measures should be explored to ensure the unreacted active CaO fully carbonatPd river the extended Ioonin cycles.展开更多
基金Project(21501007)supported by the National Natural Science Foundation of ChinaProject(2016GY-226)supported by the Industrial Science and Technology Plan in Shaanxi Province of China+1 种基金Project(ZK15044)supported by the Doctoral Scientific Research Starting Foundation of Baoji University of Arts and Sciences,ChinaProject(201610721039)supported by Undergraduate Training Programs for Innovation and Entrepreneurship,China
文摘The KxNa1-xNbO3 nanopowders with cubic-like morphology and an average size of about 50 nm were synthesized by sol-gel auto-combustion method.And then,the ceramics were prepared and the phase transition,microstructure and electrical properties of the KxNa1-xNbO3 ceramics were investigated.Pure perovskite phases of the KxNa1-xNbO3 ceramics were confirmed by XRD patterns and the K0.50Na0.50NbO3 ceramics show the coexistence of orthorhombic and monoclinic structures.SEM micrographs show that all samples have bimodal grain size distributions and the number of the small grains decrease with increasing K+content in the bimodal grain size distribution system.The K0.50Na0.50NbO3 ceramics with the uniform grain size and the maximum density show excellent electrical properties withεr=467.40,tanδ=0.020,d33=128 pC/N and kp=0.32 at the room temperature,demonstrating that the properties of the K0.50Na0.50NbO3 powers prepared by sol-gel auto-combustion are excellent and the ceramics are promising lead-free piezoelectric materials.
基金Supported by the National Natural Science Foundation of China(51276210,50906030,31301586)the Partial Financial Grant of North China University of Water Resources and Electric Power(201012)the National Basic Research Program of China(2011CB707301)
文摘Calcium looping method has been considered as one of the efficient options to capture C02 in the combustion Ilue gas. CaO-based sorbent is the basis for application of calcium looping and should be subjected to the severe calcination condition so as to obtain the concentrated C02 stream. In this research, CaO/CaZrO3 sorbents were synthesized using the sol-gel combustion synthesis （SGCS） method with urea as fuel. The cyclic reaction performance of the synthesized sorbents was evaluated on a lab-scaled reactor system through calcination at 950 ℃ in a pure C02 atmosphere and carbonation at 650 ℃ in the 15% （by volume） C02. The mass ratio of CaO to CaZr03 as 8：2 （designated as CasZr2） was screened as the best option among all the synthesized CaO sorbents for its high CO2 capture capacity and carbonation conversion at the initial cycle. And then a gradual decay in the C02 capture capacity was observed at the following 10 successive cycles, but hereafter stabilized throughout the later cycles. Furthermore, structural evolution of the carbonated CasZr2 over the looping cycles was investigated. With increasing looping cycles, the pore peak and mean grain size of the carbonated CasZr2 sorbent shifted to the bigger direction but both the surface area （SA） ratio and surface fractal dimension Ds decreased. Finally, morphological transformation of the carbonated CasZr2 was observed. Agglomeration and edge rounding of the newly formed CaC03 grains were found as aggravated at the cyclic carbonation stage. As a result, carbonation of CasZr2 with C02 was observed only confined to the external active CaO by the fast formation of the CaC03 shell outside, which occluded the further carbonation of the unreacted CaO inside. Therefore, enough attention should be paid to the carbonation stage and more effective activation measures should be explored to ensure the unreacted active CaO fully carbonatPd river the extended Ioonin cycles.
