CO2 is a major component of the greenhouse gases, which causes the global warming. To reduce CO2 gas, high activity nanosized Ni＋2 substituted Fe2TiO5 samples were synthesized by conventional ceramic method. The effe...CO2 is a major component of the greenhouse gases, which causes the global warming. To reduce CO2 gas, high activity nanosized Ni＋2 substituted Fe2TiO5 samples were synthesized by conventional ceramic method. The effect of the composition of the synthesized ferrite on the H2-reduction and CO2-catalytic decomposition was investigated. Fe2TiO5 （iron titanate） phase that has a nanocrystallite size of -80 nm is formed as a result of heating Fe2O3 and TiO2 while the addition of NiO leads to the formation of new phases （-80 nm） NiTiO3 and NiFe2O4, but the mixed solid of NiO and Fe2O3 results in the formation of NiFe2O4 only. Samples with Ni^＋2=0 shows the lowest reduction extent （20%）; as the extent of Ni＋2 increases, the extent of reduction increases. The increase in the reduction percent is attributed to the presence of NiTiO3 and NiFe2O4 phases, which are more reducible phases than Fe2TiO5. The CO2 decomposition reactions were monitored by thermogravimetric analysis （TGA） experiments. The oxidation of the H2-reduced Ni＋2 substituted Fe2TiO5 at 500℃ was investigated. As Ni^＋2 increases, the rate of reoxidation increases. Samples with the highest reduction extents gave the highest reoxidation extent, which is attributed to the highly porous nature and deficiency in oxygen due to the presence of metallic Fe, Ni and/or FeNi alloy. X-ray diffraction （XRD） and transmission electron microscopy （TEM） of oxidized samples show also the presence of carbon in the sample containing Ni＋2〉0, which appears in the form of nanotubes （25 nm）.展开更多
Fe2O3, TiO2, CuO and ZnO powders were mixed according to the formula of （1-x）TiO2 xCuO-Fe2O3 or （1-x）TiO2 xZnO-Fe2O3 （x=0, 0.2 0.4, 0.6, 0.8, 1）, and well ball-milled with H2O for 3 h to ensure homogeneity of th...Fe2O3, TiO2, CuO and ZnO powders were mixed according to the formula of （1-x）TiO2 xCuO-Fe2O3 or （1-x）TiO2 xZnO-Fe2O3 （x=0, 0.2 0.4, 0.6, 0.8, 1）, and well ball-milled with H2O for 3 h to ensure homogeneity of the powdered solids, then fired at 1200℃ for 4 h. The fired samples were reduced at 500℃ with hydrogen gas. The reduced samples were subjected to recalcination at 500℃ in CO2 atmosphere. Both of fired, reduced and calcined samples were characterized by X-ray diffraction, vibrating sample magnetometry, reflected light microscopy and scanning electron microscopy. Different phases were formed after firing of Cu^＋2 or Zn^2＋ substituted Fe2TiO5. Magnetization （Bs） of the formed phases after firing are very low corresponding to diluted magnetic semiconductors （DMS） and increases with increasing the substituted cations （Cu^＋2 or Zn^2＋）. The reduction of the fired samples enhanced the Bs values whereas the reducibility increases with increasing the Cu^＋2 or Zn^2＋ content. Samples show different tendency toward CO2 decomposition which is very important for environmental minimization for CO2.展开更多
Recent advances in the production of carbon nanotubes （CNTs） are reviewed with an emphasis on the use of carbon dioxide （CO2） as a sole source of carbon. Compared to the most widely used carbon precursors such as ...Recent advances in the production of carbon nanotubes （CNTs） are reviewed with an emphasis on the use of carbon dioxide （CO2） as a sole source of carbon. Compared to the most widely used carbon precursors such as graphite, methane, acetylene, ethanol, ethylene, and coal-derived hydrocarbons, CO2 is competitively cheaper with relatively high carbon yield content. However, CNT synthesis from CO2 is a newly emerging technology, and hence it needs to be ex- plored further. A theoretical and analytical comparison of the cur- rently existing CNT-CO2 synthesis techniques is given including a review of some of the process parameters （i.e., temperature, pres- sure, catalyst, etc.） that affect the CO2 reduction rate. Such analysis indicates that there is still a fundamental need to further explore the following aspects so as to realize the full potential of CO2 based CNT technology： （1） the CNT-CO2 synthesis and formation mechanism, （2） catalytic effects of transitional metals and mechanisms, （3） uti- lization of metallocenes in the CNT-CO2 reactions, （4） applicability of ferrite-organometallic compounds in the CNT-CO2 synthesis reactions, and （5） the effects of process parameters such as temperature, etc.展开更多
Chemical looping technology holds great potential on efficient CO2 splitting with much higher CO production and CO2 splitting rate than photocatalytic processes.Conventional oxygen carrier requires high temperature(ty...Chemical looping technology holds great potential on efficient CO2 splitting with much higher CO production and CO2 splitting rate than photocatalytic processes.Conventional oxygen carrier requires high temperature(typically 850–1000°C)to ensure sufficient redox activity,but the stable and high CO2 conversion is favored at a lower temperature,leading to the degrading on the reaction kinetics as well as the low CO production and CO2 splitting rate.In this paper,we prepared several ternary spinels and demonstrated their performance for chemical looping CO2 splitting at moderate temperatures.Using the promotion effect of Cu to cobalt ferrite reduction and reversible phase change of the reduced metals,Cu0.4 Co0.6 Fe2 O4 exhibits high CO2 splitting rate(144.6μmol g–1 min–1)and total CO production(9100μmol g–1)at 650°C.The high performance of this earth-abundant spinel material is also consistent in repeated redox cycles,enabling their potential in industrial use.展开更多
Chemical looping dry reforming（CLDR） is an innovative technology for CO2 utilization using the chemical looping principle.The CLDR process consists of three stages,i.e.CH4 reduction,CO2 reforming,and air oxidation.S...Chemical looping dry reforming（CLDR） is an innovative technology for CO2 utilization using the chemical looping principle.The CLDR process consists of three stages,i.e.CH4 reduction,CO2 reforming,and air oxidation.Spinel nickel ferrite（NiFe2O4） was prepared and its multi-cycle performance as an oxygen carrier for CLDR was experimentally investigated.X-ray diffraction（XRD） and Laser Raman spectroscopy showed that a pure spinel crystalline phase（NiFe2O4） was obtained by a parallel flow co-precipitating method.NiFe2O4was reduced into Fe-Ni alloy and wustite（FexO） during the CH4 reduction process.Subsequent oxidation of the reduced oxygen carrier was performed with CO2 as an oxidant to form an intermediate state：a mixture of spinel Ni（1-x）Fe（2＋x）O4,Fe（2＋y）O4 and metallic Ni.And CO was generated in parallel during this stage.Approximate 185 mL of CO was generated for 1 g spinel NiFe2O4 in a single cycle.The intermediate oxygen carrier was fully oxidized in the air oxidation stage to form a mixture of Ni（1＋x）Fe（2-x）O4 and Fe2O3.Although the original state of oxygen carrier（NiFe2O4） was not fully regenerated and agglomeration was observed,a good recyclability was shown in 10 successive redox cycles.展开更多
采用普通陶瓷工艺制备了Sm^(3+)掺杂的Co_2Z型平面六角铁氧体,研究了Sm^(3+)掺杂Co_2Z型铁氧体材料的组织结构和吸波性能。结果表明,掺杂一定量Sm^(3+)的铁氧体相结构仍以Co_2Z型六角晶系相为主相,但出现了呈颗粒状弥散分布的富Sm相。掺...采用普通陶瓷工艺制备了Sm^(3+)掺杂的Co_2Z型平面六角铁氧体,研究了Sm^(3+)掺杂Co_2Z型铁氧体材料的组织结构和吸波性能。结果表明,掺杂一定量Sm^(3+)的铁氧体相结构仍以Co_2Z型六角晶系相为主相,但出现了呈颗粒状弥散分布的富Sm相。掺杂Sm^(3+)样品的吸波性能明显优于未掺杂Sm^(3+)样品,在频率为6.3 GHz时,其最大反射损耗可达到-20 d B,耗损大于10 d B的频带带宽为5 GHz,具有较宽的吸收频带。吸波涂层的附着强度均大于10 MPa,具有良好的力学性能。展开更多
文摘CO2 is a major component of the greenhouse gases, which causes the global warming. To reduce CO2 gas, high activity nanosized Ni＋2 substituted Fe2TiO5 samples were synthesized by conventional ceramic method. The effect of the composition of the synthesized ferrite on the H2-reduction and CO2-catalytic decomposition was investigated. Fe2TiO5 （iron titanate） phase that has a nanocrystallite size of -80 nm is formed as a result of heating Fe2O3 and TiO2 while the addition of NiO leads to the formation of new phases （-80 nm） NiTiO3 and NiFe2O4, but the mixed solid of NiO and Fe2O3 results in the formation of NiFe2O4 only. Samples with Ni^＋2=0 shows the lowest reduction extent （20%）; as the extent of Ni＋2 increases, the extent of reduction increases. The increase in the reduction percent is attributed to the presence of NiTiO3 and NiFe2O4 phases, which are more reducible phases than Fe2TiO5. The CO2 decomposition reactions were monitored by thermogravimetric analysis （TGA） experiments. The oxidation of the H2-reduced Ni＋2 substituted Fe2TiO5 at 500℃ was investigated. As Ni^＋2 increases, the rate of reoxidation increases. Samples with the highest reduction extents gave the highest reoxidation extent, which is attributed to the highly porous nature and deficiency in oxygen due to the presence of metallic Fe, Ni and/or FeNi alloy. X-ray diffraction （XRD） and transmission electron microscopy （TEM） of oxidized samples show also the presence of carbon in the sample containing Ni＋2〉0, which appears in the form of nanotubes （25 nm）.
文摘Fe2O3, TiO2, CuO and ZnO powders were mixed according to the formula of （1-x）TiO2 xCuO-Fe2O3 or （1-x）TiO2 xZnO-Fe2O3 （x=0, 0.2 0.4, 0.6, 0.8, 1）, and well ball-milled with H2O for 3 h to ensure homogeneity of the powdered solids, then fired at 1200℃ for 4 h. The fired samples were reduced at 500℃ with hydrogen gas. The reduced samples were subjected to recalcination at 500℃ in CO2 atmosphere. Both of fired, reduced and calcined samples were characterized by X-ray diffraction, vibrating sample magnetometry, reflected light microscopy and scanning electron microscopy. Different phases were formed after firing of Cu^＋2 or Zn^2＋ substituted Fe2TiO5. Magnetization （Bs） of the formed phases after firing are very low corresponding to diluted magnetic semiconductors （DMS） and increases with increasing the substituted cations （Cu^＋2 or Zn^2＋）. The reduction of the fired samples enhanced the Bs values whereas the reducibility increases with increasing the Cu^＋2 or Zn^2＋ content. Samples show different tendency toward CO2 decomposition which is very important for environmental minimization for CO2.
文摘Recent advances in the production of carbon nanotubes （CNTs） are reviewed with an emphasis on the use of carbon dioxide （CO2） as a sole source of carbon. Compared to the most widely used carbon precursors such as graphite, methane, acetylene, ethanol, ethylene, and coal-derived hydrocarbons, CO2 is competitively cheaper with relatively high carbon yield content. However, CNT synthesis from CO2 is a newly emerging technology, and hence it needs to be ex- plored further. A theoretical and analytical comparison of the cur- rently existing CNT-CO2 synthesis techniques is given including a review of some of the process parameters （i.e., temperature, pres- sure, catalyst, etc.） that affect the CO2 reduction rate. Such analysis indicates that there is still a fundamental need to further explore the following aspects so as to realize the full potential of CO2 based CNT technology： （1） the CNT-CO2 synthesis and formation mechanism, （2） catalytic effects of transitional metals and mechanisms, （3） uti- lization of metallocenes in the CNT-CO2 reactions, （4） applicability of ferrite-organometallic compounds in the CNT-CO2 synthesis reactions, and （5） the effects of process parameters such as temperature, etc.
基金National Natural Science Foundation of China(Grant No.51706041)the National Natural Science Foundation of China(NSFC)Projects(Grant No.51661145011)the National Science Foundation for Distinguished Young Scholars of China(Grant No.51525601)。
文摘Chemical looping technology holds great potential on efficient CO2 splitting with much higher CO production and CO2 splitting rate than photocatalytic processes.Conventional oxygen carrier requires high temperature(typically 850–1000°C)to ensure sufficient redox activity,but the stable and high CO2 conversion is favored at a lower temperature,leading to the degrading on the reaction kinetics as well as the low CO production and CO2 splitting rate.In this paper,we prepared several ternary spinels and demonstrated their performance for chemical looping CO2 splitting at moderate temperatures.Using the promotion effect of Cu to cobalt ferrite reduction and reversible phase change of the reduced metals,Cu0.4 Co0.6 Fe2 O4 exhibits high CO2 splitting rate(144.6μmol g–1 min–1)and total CO production(9100μmol g–1)at 650°C.The high performance of this earth-abundant spinel material is also consistent in repeated redox cycles,enabling their potential in industrial use.
基金the financial support by the National Natural Science Foundation of China(51406214 and51406208)supported by the Natural science Foundation of Guangdong Province(2015A030313719)the Science&Technology Research Project of Guangdong Province(2013B050800008)
文摘Chemical looping dry reforming（CLDR） is an innovative technology for CO2 utilization using the chemical looping principle.The CLDR process consists of three stages,i.e.CH4 reduction,CO2 reforming,and air oxidation.Spinel nickel ferrite（NiFe2O4） was prepared and its multi-cycle performance as an oxygen carrier for CLDR was experimentally investigated.X-ray diffraction（XRD） and Laser Raman spectroscopy showed that a pure spinel crystalline phase（NiFe2O4） was obtained by a parallel flow co-precipitating method.NiFe2O4was reduced into Fe-Ni alloy and wustite（FexO） during the CH4 reduction process.Subsequent oxidation of the reduced oxygen carrier was performed with CO2 as an oxidant to form an intermediate state：a mixture of spinel Ni（1-x）Fe（2＋x）O4,Fe（2＋y）O4 and metallic Ni.And CO was generated in parallel during this stage.Approximate 185 mL of CO was generated for 1 g spinel NiFe2O4 in a single cycle.The intermediate oxygen carrier was fully oxidized in the air oxidation stage to form a mixture of Ni（1＋x）Fe（2-x）O4 and Fe2O3.Although the original state of oxygen carrier（NiFe2O4） was not fully regenerated and agglomeration was observed,a good recyclability was shown in 10 successive redox cycles.
文摘采用普通陶瓷工艺制备了Sm^(3+)掺杂的Co_2Z型平面六角铁氧体,研究了Sm^(3+)掺杂Co_2Z型铁氧体材料的组织结构和吸波性能。结果表明,掺杂一定量Sm^(3+)的铁氧体相结构仍以Co_2Z型六角晶系相为主相,但出现了呈颗粒状弥散分布的富Sm相。掺杂Sm^(3+)样品的吸波性能明显优于未掺杂Sm^(3+)样品,在频率为6.3 GHz时,其最大反射损耗可达到-20 d B,耗损大于10 d B的频带带宽为5 GHz,具有较宽的吸收频带。吸波涂层的附着强度均大于10 MPa,具有良好的力学性能。
