The pressurized combustion experiments of bituminous coal and lignite under air and O2/CO2 atmospheres were conducted to study the influences of pressure and atmosphere on combustion and the CO, NO, SO2 release proces...The pressurized combustion experiments of bituminous coal and lignite under air and O2/CO2 atmospheres were conducted to study the influences of pressure and atmosphere on combustion and the CO, NO, SO2 release process. Two indices, the maximum concentration and the total emission, were applied to quantitatively evaluate the influence of several different operating parameters such as pressure, atmosphere and temperature on the formation of NO and SO2 during coal combustion in the fluidized bed. The experimental results show that the releasing profiles of CO, NO and SO2 during coal combustion under a pressurized oxy- fuel atmosphere are similar to those under a pressurized air atmosphere, and the curves of measured gas components are all unimodal. Under the oxy-fuel condition, pressure increasing from 0.1 to 0.7 MPa can cause the inhibition of NO and SO2 emission. The elevation of temperature can lead to an increase in the maximum concentration and the total production of NO and SO2, and the increase under atmospheric pressure is higher than that under high pressure.展开更多
The thermogravimetric analyzer and horizontal tube furnace are used to study the effects of operation parameters such as temperature, fuel type, and oxygen concentration on the combustion and NO emission characteristi...The thermogravimetric analyzer and horizontal tube furnace are used to study the effects of operation parameters such as temperature, fuel type, and oxygen concentration on the combustion and NO emission characteristics of the rice husk, rice straw, and peanut shell in the O2/CO2 atmosphere. The results show that the combustion performances of volatile matter and fixed carbon of the three biomasses increase with the increase in the 02 content. The mean NO emission increases sharply when the reaction temperature increases from 700 to 800℃. However, it increases slightly when the temperature exceeds 800 ℃. Meanwhile, the mean NO emission and nitrogen conversion decrease with the increase in the nitrogen content in biomass. The mean NO emission changes little with different oxygen concentrations, and the NO emissions of the three biomasses are all lower than the requirement for the minimum NO emission. Increasing the oxygen concentration favors the biomass combustion in the O2/CO2 atmosphere, and oxygen concentration has little effect on the NO emission.展开更多
Engineering the morphology of the support is effective in tuning the redox properties of active metals for efficient catalytic methane combustion via tailoring the metal-support interaction.Herein,uniform Ir nanoparti...Engineering the morphology of the support is effective in tuning the redox properties of active metals for efficient catalytic methane combustion via tailoring the metal-support interaction.Herein,uniform Ir nanoparticles supported on anatase TiO_(2)with different morphologies predominantly exposing{100},{101},and{001}planes were synthesized and tested for methane combustion.The CH_(4) catalytic activity shows a remarkable TiO_(2)-facet-dependent effect and follows the order of Ir/TiO_(2)-{100}>Ir/TiO_(2)-{101}>>Ir/TiO_(2)-{001}.Detailed characterizations and DFT calculations reveal that compared with Ir-TiO_(2)-{101}and Ir-TiO_(2)-{001}interfaces,the superior Ir-TiO_(2)-{100}interface facilitates the generation of electron-rich Ir species through more profound charge transfer from TiO_(2)-{100}to Ir atoms.The electron-rich Ir structure,featuring abundant defect oxygen vacancies,significantly enhances the redox properties of active Ir species and reduces the activation energy for breaking the initial C-H bond in CH_(4),resulting in the superior catalytic activity for methane combustion.These findings deepen fundamental insights into the TiO_(2)-facet-dependent reactivity of different Ir/TiO_(2)nanomaterials in methane oxidation and pave the way for designing efficient Ir-based methane oxidation catalysts.展开更多
为探究稻茬小麦深施肥“一基一追”机艺融合技术的增产增效减排机制,2021—2024年在长江下游南通稻茬麦区开展大田试验。试验采用缓释掺混肥料(SRF,N∶P_(2)O_(5)∶K_(2)O=26∶12∶12)和普通尿素(U,46%N),结合自主研发的2BFGK-12(6)260...为探究稻茬小麦深施肥“一基一追”机艺融合技术的增产增效减排机制,2021—2024年在长江下游南通稻茬麦区开展大田试验。试验采用缓释掺混肥料(SRF,N∶P_(2)O_(5)∶K_(2)O=26∶12∶12)和普通尿素(U,46%N),结合自主研发的2BFGK-12(6)260全秸秆茬地洁区旋耕智能施肥播种机和3ZF-4(200)中耕追肥机,设置7种施肥模式(30 cm+15 cm宽窄行种植):以尿素4次分施(N 240 kg hm^(-2),基肥∶分蘖肥∶拔节肥∶孕穗肥=5∶1∶2∶2,窄行基施,追肥全田撒施)为对照(CK);减氮15%(N 204 kg hm^(-2))条件下设置6种处理:M_(1)(100%SRF窄行基施);M_(2)(60%SRF窄行基施+40%U拔节期窄行撒施);M_(3)(60%SRF窄行基施+40%U返青期宽行条施);M_(4)(60%SRF窄行基施+40%SRF返青期窄行撒施);M_(5)(60%SRF窄行基施+40%SRF返青期宽行条施);M_(4+5)(60%SRF窄行基施+20%SRF返青期宽行条施+20%SRF返青期窄行撒施)。研究比较不同施肥模式对小麦产量效益、根系形态生理、氮素利用效率及N_(2)O排放的影响。结果表明,与CK相比,M_(2)~M_(5)处理提高了小麦产量(4.0%~19.0%)和经济效益(13.7%~35.7%),其中M_(4)和M_(5)处理表现最优,分别增产14.1%和19.0%,经济效益提升34.5%和35.7%。这些处理明显改善了根系特性(根干重密度增加9.7%~111.8%,根系活力和氧化力分别提高6.8%~52.0%和4.2%~44.2%),降低N_(2)O累积排放量22.6%~34.5%,提高0~20 cm土层硝态氮含量11.2%~40.0%。在氮素利用方面,M_(2)~M_(5)处理均提高了籽粒氮素积累量、花后氮素积累量及其对籽粒氮素的贡献率,氮肥利用效率指标(包括偏生产力、农学效率和表观利用率)分别显著提升了22.4%~40.0%、29.7%~74.3%和9.41~18.77个百分点。值得注意的是,M_(4)和M_(5)处理表现出最优的综合效益:N_(2)O累积排放量降幅最大(分别达27.0%和34.5%),氮肥表观利用率2季均维持在43.0%以上(均值分别为43.5%和46.8%),同时在生育后期保持较高的根系活性和耕层无机氮含量。相比之下,M_(1)处理虽然实现了最大的N_(2)O减排效果(降幅35.9%),但导致减产10.4%和经济效益下降10.8%,且氮肥利用效率呈现不稳定的年际变化特征。而优化处理M_(4+5)进一步改善了根系形态生理特性,并提高氮肥表观利用率和籽粒氮素积累量。综上,减氮15%条件下(N 204 kg hm^(-2)),缓混肥2次施用处理(M_(4)和M_(5))能实现产量、经济效益、氮肥利用效率和N_(2)O减排的协同提高,并以追肥深施处理(M_(5))效应更强。本研究为稻茬小麦缓释肥减氮优化高效应用提供重要理论依据。展开更多
A 20 wt% Ni/bentonite catalyst was prepared by a solution combustion synthesis (SCS), which exhibited higher activity for the CO_2methanation than that of an impregnation method (IPM), and the catalyst prepared by SCS...A 20 wt% Ni/bentonite catalyst was prepared by a solution combustion synthesis (SCS), which exhibited higher activity for the CO_2methanation than that of an impregnation method (IPM), and the catalyst prepared by SCS showed a CO_2 conversion of 85% and a CH4selectivity of 100% at 300 °C, atmospheric pressure, and 3600 ml·(g cat)-1·h-1, and the catalyst exhibited stable within a 110-h reaction. The results showed higher me- tallic Ni dispersion, smaller Ni particle size, larger specific surface area and lower reduction temperature in the Ni/ bentonite prepared by SCS than that of IPM. And the Ni/bentonite prepared by the SCS moderated the interaction between NiO and bentonite.展开更多
A series of Ni/ZrO_2 catalysts were synthesized by urea combustion method for CO_2 methanation.The effects of zirconium precursors and urea dosage on the structure and catalytic performance of the catalysts were teste...A series of Ni/ZrO_2 catalysts were synthesized by urea combustion method for CO_2 methanation.The effects of zirconium precursors and urea dosage on the structure and catalytic performance of the catalysts were tested.Results showed that the Ni/ZrO_2–O catalyst derived from zirconium oxynitrate hydrate exhibited better catalytic activity than the Ni/ZrO_2 catalyst because of its higher Ni dispersion and smaller Ni particle size.In addition,the urea dosage significantly influenced the low-temperature activity of the catalysts by affecting the metal–support interaction,Ni dispersion,and Ni particle size.The Ni/ZrO_2–O-0.4 catalyst with a urea-to-nitrate molar ratio of 0.4 exhibited the best catalytic activity owing to its moderate metal–support interaction,highest Ni dispersion,and smallest Ni particle size,achieving 69.2% CO_2 conversion and 100% CH_4 selectivity at 300℃,0.1 MPa,and a weight hour space velocity(WHSV)of 50,000 mL/(g·h).Moreover,the urea combustion method can lead to the entire phase transformation from monoclinic ZrO_2 to tetragonal ZrO_2 accompanied by the incorporation of oxygen vacancies in the ZrO_2 lattice.This phenomenon can also be related to the high catalytic activity of the as-prepared catalysts.展开更多
The temperature dependence on the reaction of desulfurization reagent CaCO3 and SO2 in O2/CO2 coal combustion was investigated by thcrmogravimetric analysis, X-ray diffraction measurement and pore structure analysis. ...The temperature dependence on the reaction of desulfurization reagent CaCO3 and SO2 in O2/CO2 coal combustion was investigated by thcrmogravimetric analysis, X-ray diffraction measurement and pore structure analysis. The results show that the conversion of the reaction of CaCO3 and SO2 in air is higher at 500-1 100 ℃ and lower at 1 200 ℃ compared with that in O2/CO2 atmosphere. The conversion can be increased by increasing the concentration of SO2, which causes the inhibition of CaSO4 decomposition and shifting of the reaction equilibrium toward the products. XRD analysis of the product shows that the reaction mechanism of CaCO3 and SO2 differs with temperature in O2/CO2 atmosphere, i.e. CaCO3 directly reacts with SO2 at 500 ℃ and CaO from CaCO3 decomposition reacts with SO2 at 1 000 ℃. The pore analysis of the products indicates that the maximum specific surface area of the products accounts for the highest conversion at 1 100 ℃ in O2/CO2 atmosphere. The results reveal that the effect of the atmosphere on the conversion is temperature dependence.展开更多
At present monoethanolamine(MEA) remains as the standard industrial solvent for CO_2 capture processes. But due to the degradation and high energy consumption problems of MEA, new efficient solvents should be found. I...At present monoethanolamine(MEA) remains as the standard industrial solvent for CO_2 capture processes. But due to the degradation and high energy consumption problems of MEA, new efficient solvents should be found. In the present work, the absorption and regeneration performance of a hybrid solvent MEA-methanol was studied and compared to the aqueous solutions of monoethanolamine(MEA), diethanolamine(DEA) and triethanolamine(TEA) in a bubbling reactor. Also the performance of MEA-methanol solutions(including the absorption performance, regeneration performance,cyclic absorption performance, density and viscosity) was studied with different MEA concentrations. A pilot-plant CO_2 capture test bed was used to study the potential of MEA-methanol to replace aqueous MEA in industrial use. The results showed that the initial absorption rate of MEA-methanol solvent is the fastest compared with other solvents. The 30% MEA-methanol had a faster mass transfer coefficient, a higher CO_2 absorption efficiency and a lower regeneration energy consumption than aqueous MEA. And through the study of the reaction heat of CO_2 into MEA-methanol and aqueous MEA,it can be concluded that the desorption heat of rich MEA-methanol is only about 30% of rich aqueous MEA solvent in the regeneration process which showed that 30% MEA-methanol solvent is a promising candidate for CO_2 capture.展开更多
Benzylamine(BZA) has been identified as a promising candidate for CO_2 capture process; however the evaluation of BZA in the packed column was very few. Thus, in this work, the absorption and regeneration performance ...Benzylamine(BZA) has been identified as a promising candidate for CO_2 capture process; however the evaluation of BZA in the packed column was very few. Thus, in this work, the absorption and regeneration performance of unblended BZA solvent as well as a series of amine concentrations and ratios in the formulations were studied using a semibatch bubbling reactor. And due to the formation of ivory-white precipitates in solvents containing higher BZA ratios, a 4:1 molar ratio of MEA/BZA mixed solvent was used to study its performance in a pilot-scale test bed. The results showed that a higher BZA ratio in the MEA/BZA mixed solvent resulted in a faster absorption rate, a higher mass transfer and heat transfer rate and a better cyclic performance, but the mass transfer rate of BZA decreased more quickly than MEA with the increase of CO_2 loading of the solvents. In addition, at high CO_2 loading in the MEA/ BZA mixed solvent with a molar ratio of 4:1, the ivory-white precipitates were generated which could cause blockage of the packing in the absorber, the stripper and the liquid pipelines.展开更多
SO2 release and removal were studied under both the air and oxy-fuel combustion conditions using an anthracite coal from the Jincheng mine in China on a bench-scale fluidized bed combustor （FBC）. Special attention w...SO2 release and removal were studied under both the air and oxy-fuel combustion conditions using an anthracite coal from the Jincheng mine in China on a bench-scale fluidized bed combustor （FBC）. Special attention was paid to the effects of the combustion atmosphere, 02 concentration, bed temperature, and limestone addition. The released amount of SO2 was clearly higher under 30% 02/70% CO2 than that of the air atmosphere. As the O2 concentration in O2/CO2 mixture increased from 21% to 40%, the released amount of SO2 increased significantly, but then it decreased when the 02 concentration increased up to 50%. The bed temperature from 860 to 920 ℃ has no obvious influence on the the SO2 release but shows a strong influence on the desulfurization with limestone in both oxy-fuel and air conditions. The maximum SO2 removal efficiency appears to be at 880 to 900 ℃ for both the air and oxy-fuel combustion conditions.展开更多
The non-grinding long afterglow material SrAl2O4：Eu^2＋ , Dy^3＋ was prepared by combustion method in home mierowave oven direetly, after dispersant, frother, eomburent, and mineralizer were added into the reacting s...The non-grinding long afterglow material SrAl2O4：Eu^2＋ , Dy^3＋ was prepared by combustion method in home mierowave oven direetly, after dispersant, frother, eomburent, and mineralizer were added into the reacting system. XRD analysis showed that the powders were nearly pure SrAl2O4 phase with few other phases, and the size of the grain was 41.1 nm. Fluoreseenee speetrum results indieated that there were 2 exeitation peaks loeated at 345 and 400 nm, and the emission peak loeated at 516 nm, afterglow lasted up to 30 min or more. The mierowave eombustion method has advantages of less time, low temperature and no grinding process, and the material made by the method has good luminescent property.展开更多
Ni-Y2O3 nanocomposite powder with uniform distribution of fine oxide particles in the metal matrix was successfully fabricated via solution combustion process followed by hydrogen reduction. The combustion behavior wa...Ni-Y2O3 nanocomposite powder with uniform distribution of fine oxide particles in the metal matrix was successfully fabricated via solution combustion process followed by hydrogen reduction. The combustion behavior was investigated by DTA-TG analysis. The influence of urea to nickel nitrate（U/Ni） ratio on the combustion behavior and morphology evolution of the combusted powder was investigated. The morphological characteristics and phase transformation of the combusted powder and the reduced powder were characterized by FESEM, TEM and XRD. The HRTEM image of Ni-Y2O3 nanocomposite powder indicated that Y2O3 particles with average particle size of about 10 nm dispersed uniformly in the nickel matrix.展开更多
Activity and stability of 1%Pd-0.2%Pt/Al2O3 and 1%Pd-0.2%Pt/0.6%Ce/Al2O3 catalysts prepared by impregnation method for catalytic combustion of methane in air were investigated. The catalysts before and after reaction ...Activity and stability of 1%Pd-0.2%Pt/Al2O3 and 1%Pd-0.2%Pt/0.6%Ce/Al2O3 catalysts prepared by impregnation method for catalytic combustion of methane in air were investigated. The catalysts before and after reaction were characterized by BET, CO chemisorption, XRD and XPS techniques. Results showed that the presence of Ce significantly increased the activity and thermal stability of the Pd-Pt/Al2O3 catalyst towards methane combustion, which could be attributed to more highly-dispersed active PdO particles over the Pd-Pt/Ce/Al2O3 catalyst surface as well as the retarded sintering of PdO and the maintained oxidized state of surface Pd during the combustion process in the presence of Ce.展开更多
Galvanic deposition method was used to prepare the Pd/Ni-Al2O3-GD catalyst for the combustion of methane under lean conditions. The new catalyst and compared catalysts （Pd/Al2O3-IW, Pd-Ni/Al2O3-IW, Pd/Ni-Al2O3-IW） p...Galvanic deposition method was used to prepare the Pd/Ni-Al2O3-GD catalyst for the combustion of methane under lean conditions. The new catalyst and compared catalysts （Pd/Al2O3-IW, Pd-Ni/Al2O3-IW, Pd/Ni-Al2O3-IW） prepared by incipient wetness impregnation were characterized by N2-physisorption, XRD and TEM to clarify particle size and size distribution of palladium species. Combined O2-TPD and XPS results with the catalytic data, it shows that the surface palladium species with low valence exhibits better combustion performance due to their stronger interaction with support. The results indicate that the galvanic deposition method is an effective route to prepare efficient catalyst for methane combustion, and it also provides useful information for improving the present commercial catalyst.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
Blue-green luminescent BaAl2O4：Eu2＋,Dy3＋ phosphor powders were synthesized via combustion synthesis method assisted by microwave irradiation in air. The phosphors were characterized by X-ray diffraction （XRD）, sc...Blue-green luminescent BaAl2O4：Eu2＋,Dy3＋ phosphor powders were synthesized via combustion synthesis method assisted by microwave irradiation in air. The phosphors were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and fluorescence spectrophotometer. The XRD results revealed that when the concentration of urea was over 3 times higher than theoretical quantities, a BaAl2O4 single hexagonal phase was obtained. The SEM results revealed that the surface of the BaAl2O4：Eu2＋,Dy3＋ powder samples showed lots of voids and pores. The BaAl2O4：Eu2＋,Dy3＋ phosphors exhibited a broad emission band of main peak at 496 nm and a shoulder peak at 426 nm under excitation of 337 nm. The BaAl2O4：Eu2＋,Dy3＋ phosphors at the Eu2＋ concentration of 1 mol.% showed the strongest luminescent intensity. Long afterglow phosphorescence was observed in the dark with naked eyes after the removal of the excitation source.展开更多
基金The National Natural Science Foundation of China(No.51206023)the National Key Basic Research Program of China(973 Program)(No.2011CB707301-3)the Fundamental Research Funds for the Central Universities
文摘The pressurized combustion experiments of bituminous coal and lignite under air and O2/CO2 atmospheres were conducted to study the influences of pressure and atmosphere on combustion and the CO, NO, SO2 release process. Two indices, the maximum concentration and the total emission, were applied to quantitatively evaluate the influence of several different operating parameters such as pressure, atmosphere and temperature on the formation of NO and SO2 during coal combustion in the fluidized bed. The experimental results show that the releasing profiles of CO, NO and SO2 during coal combustion under a pressurized oxy- fuel atmosphere are similar to those under a pressurized air atmosphere, and the curves of measured gas components are all unimodal. Under the oxy-fuel condition, pressure increasing from 0.1 to 0.7 MPa can cause the inhibition of NO and SO2 emission. The elevation of temperature can lead to an increase in the maximum concentration and the total production of NO and SO2, and the increase under atmospheric pressure is higher than that under high pressure.
基金The Natural Science Foundation of Anhui Province(No.1508085ME73)the Open Foundation of Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education(No.201406)
文摘The thermogravimetric analyzer and horizontal tube furnace are used to study the effects of operation parameters such as temperature, fuel type, and oxygen concentration on the combustion and NO emission characteristics of the rice husk, rice straw, and peanut shell in the O2/CO2 atmosphere. The results show that the combustion performances of volatile matter and fixed carbon of the three biomasses increase with the increase in the 02 content. The mean NO emission increases sharply when the reaction temperature increases from 700 to 800℃. However, it increases slightly when the temperature exceeds 800 ℃. Meanwhile, the mean NO emission and nitrogen conversion decrease with the increase in the nitrogen content in biomass. The mean NO emission changes little with different oxygen concentrations, and the NO emissions of the three biomasses are all lower than the requirement for the minimum NO emission. Increasing the oxygen concentration favors the biomass combustion in the O2/CO2 atmosphere, and oxygen concentration has little effect on the NO emission.
文摘Engineering the morphology of the support is effective in tuning the redox properties of active metals for efficient catalytic methane combustion via tailoring the metal-support interaction.Herein,uniform Ir nanoparticles supported on anatase TiO_(2)with different morphologies predominantly exposing{100},{101},and{001}planes were synthesized and tested for methane combustion.The CH_(4) catalytic activity shows a remarkable TiO_(2)-facet-dependent effect and follows the order of Ir/TiO_(2)-{100}>Ir/TiO_(2)-{101}>>Ir/TiO_(2)-{001}.Detailed characterizations and DFT calculations reveal that compared with Ir-TiO_(2)-{101}and Ir-TiO_(2)-{001}interfaces,the superior Ir-TiO_(2)-{100}interface facilitates the generation of electron-rich Ir species through more profound charge transfer from TiO_(2)-{100}to Ir atoms.The electron-rich Ir structure,featuring abundant defect oxygen vacancies,significantly enhances the redox properties of active Ir species and reduces the activation energy for breaking the initial C-H bond in CH_(4),resulting in the superior catalytic activity for methane combustion.These findings deepen fundamental insights into the TiO_(2)-facet-dependent reactivity of different Ir/TiO_(2)nanomaterials in methane oxidation and pave the way for designing efficient Ir-based methane oxidation catalysts.
文摘为探究稻茬小麦深施肥“一基一追”机艺融合技术的增产增效减排机制,2021—2024年在长江下游南通稻茬麦区开展大田试验。试验采用缓释掺混肥料(SRF,N∶P_(2)O_(5)∶K_(2)O=26∶12∶12)和普通尿素(U,46%N),结合自主研发的2BFGK-12(6)260全秸秆茬地洁区旋耕智能施肥播种机和3ZF-4(200)中耕追肥机,设置7种施肥模式(30 cm+15 cm宽窄行种植):以尿素4次分施(N 240 kg hm^(-2),基肥∶分蘖肥∶拔节肥∶孕穗肥=5∶1∶2∶2,窄行基施,追肥全田撒施)为对照(CK);减氮15%(N 204 kg hm^(-2))条件下设置6种处理:M_(1)(100%SRF窄行基施);M_(2)(60%SRF窄行基施+40%U拔节期窄行撒施);M_(3)(60%SRF窄行基施+40%U返青期宽行条施);M_(4)(60%SRF窄行基施+40%SRF返青期窄行撒施);M_(5)(60%SRF窄行基施+40%SRF返青期宽行条施);M_(4+5)(60%SRF窄行基施+20%SRF返青期宽行条施+20%SRF返青期窄行撒施)。研究比较不同施肥模式对小麦产量效益、根系形态生理、氮素利用效率及N_(2)O排放的影响。结果表明,与CK相比,M_(2)~M_(5)处理提高了小麦产量(4.0%~19.0%)和经济效益(13.7%~35.7%),其中M_(4)和M_(5)处理表现最优,分别增产14.1%和19.0%,经济效益提升34.5%和35.7%。这些处理明显改善了根系特性(根干重密度增加9.7%~111.8%,根系活力和氧化力分别提高6.8%~52.0%和4.2%~44.2%),降低N_(2)O累积排放量22.6%~34.5%,提高0~20 cm土层硝态氮含量11.2%~40.0%。在氮素利用方面,M_(2)~M_(5)处理均提高了籽粒氮素积累量、花后氮素积累量及其对籽粒氮素的贡献率,氮肥利用效率指标(包括偏生产力、农学效率和表观利用率)分别显著提升了22.4%~40.0%、29.7%~74.3%和9.41~18.77个百分点。值得注意的是,M_(4)和M_(5)处理表现出最优的综合效益:N_(2)O累积排放量降幅最大(分别达27.0%和34.5%),氮肥表观利用率2季均维持在43.0%以上(均值分别为43.5%和46.8%),同时在生育后期保持较高的根系活性和耕层无机氮含量。相比之下,M_(1)处理虽然实现了最大的N_(2)O减排效果(降幅35.9%),但导致减产10.4%和经济效益下降10.8%,且氮肥利用效率呈现不稳定的年际变化特征。而优化处理M_(4+5)进一步改善了根系形态生理特性,并提高氮肥表观利用率和籽粒氮素积累量。综上,减氮15%条件下(N 204 kg hm^(-2)),缓混肥2次施用处理(M_(4)和M_(5))能实现产量、经济效益、氮肥利用效率和N_(2)O减排的协同提高,并以追肥深施处理(M_(5))效应更强。本研究为稻茬小麦缓释肥减氮优化高效应用提供重要理论依据。
基金Supported by the National Natural Science Foundation of China(21566005)the Natural Science Foundation of Guangxi Province(2016GXNSFFA380015)
文摘A 20 wt% Ni/bentonite catalyst was prepared by a solution combustion synthesis (SCS), which exhibited higher activity for the CO_2methanation than that of an impregnation method (IPM), and the catalyst prepared by SCS showed a CO_2 conversion of 85% and a CH4selectivity of 100% at 300 °C, atmospheric pressure, and 3600 ml·(g cat)-1·h-1, and the catalyst exhibited stable within a 110-h reaction. The results showed higher me- tallic Ni dispersion, smaller Ni particle size, larger specific surface area and lower reduction temperature in the Ni/ bentonite prepared by SCS than that of IPM. And the Ni/bentonite prepared by the SCS moderated the interaction between NiO and bentonite.
文摘A series of Ni/ZrO_2 catalysts were synthesized by urea combustion method for CO_2 methanation.The effects of zirconium precursors and urea dosage on the structure and catalytic performance of the catalysts were tested.Results showed that the Ni/ZrO_2–O catalyst derived from zirconium oxynitrate hydrate exhibited better catalytic activity than the Ni/ZrO_2 catalyst because of its higher Ni dispersion and smaller Ni particle size.In addition,the urea dosage significantly influenced the low-temperature activity of the catalysts by affecting the metal–support interaction,Ni dispersion,and Ni particle size.The Ni/ZrO_2–O-0.4 catalyst with a urea-to-nitrate molar ratio of 0.4 exhibited the best catalytic activity owing to its moderate metal–support interaction,highest Ni dispersion,and smallest Ni particle size,achieving 69.2% CO_2 conversion and 100% CH_4 selectivity at 300℃,0.1 MPa,and a weight hour space velocity(WHSV)of 50,000 mL/(g·h).Moreover,the urea combustion method can lead to the entire phase transformation from monoclinic ZrO_2 to tetragonal ZrO_2 accompanied by the incorporation of oxygen vacancies in the ZrO_2 lattice.This phenomenon can also be related to the high catalytic activity of the as-prepared catalysts.
基金Project(50525619) supported by the National Natural Science Foundation of ChinaProject(306012) supported by the Key Foundation of Ministry of Education of China
文摘The temperature dependence on the reaction of desulfurization reagent CaCO3 and SO2 in O2/CO2 coal combustion was investigated by thcrmogravimetric analysis, X-ray diffraction measurement and pore structure analysis. The results show that the conversion of the reaction of CaCO3 and SO2 in air is higher at 500-1 100 ℃ and lower at 1 200 ℃ compared with that in O2/CO2 atmosphere. The conversion can be increased by increasing the concentration of SO2, which causes the inhibition of CaSO4 decomposition and shifting of the reaction equilibrium toward the products. XRD analysis of the product shows that the reaction mechanism of CaCO3 and SO2 differs with temperature in O2/CO2 atmosphere, i.e. CaCO3 directly reacts with SO2 at 500 ℃ and CaO from CaCO3 decomposition reacts with SO2 at 1 000 ℃. The pore analysis of the products indicates that the maximum specific surface area of the products accounts for the highest conversion at 1 100 ℃ in O2/CO2 atmosphere. The results reveal that the effect of the atmosphere on the conversion is temperature dependence.
基金supported by the Sinopec Ningbo Engineering Co., Ltd.(No.l4850000-14-ZC0609-0003, H8XY-0032)
文摘At present monoethanolamine(MEA) remains as the standard industrial solvent for CO_2 capture processes. But due to the degradation and high energy consumption problems of MEA, new efficient solvents should be found. In the present work, the absorption and regeneration performance of a hybrid solvent MEA-methanol was studied and compared to the aqueous solutions of monoethanolamine(MEA), diethanolamine(DEA) and triethanolamine(TEA) in a bubbling reactor. Also the performance of MEA-methanol solutions(including the absorption performance, regeneration performance,cyclic absorption performance, density and viscosity) was studied with different MEA concentrations. A pilot-plant CO_2 capture test bed was used to study the potential of MEA-methanol to replace aqueous MEA in industrial use. The results showed that the initial absorption rate of MEA-methanol solvent is the fastest compared with other solvents. The 30% MEA-methanol had a faster mass transfer coefficient, a higher CO_2 absorption efficiency and a lower regeneration energy consumption than aqueous MEA. And through the study of the reaction heat of CO_2 into MEA-methanol and aqueous MEA,it can be concluded that the desorption heat of rich MEA-methanol is only about 30% of rich aqueous MEA solvent in the regeneration process which showed that 30% MEA-methanol solvent is a promising candidate for CO_2 capture.
基金supported by the Sinopec Ningbo Engineering Co. Ltd. (No.l4850000-14-ZC0609-0003,H8XY-0032)
文摘Benzylamine(BZA) has been identified as a promising candidate for CO_2 capture process; however the evaluation of BZA in the packed column was very few. Thus, in this work, the absorption and regeneration performance of unblended BZA solvent as well as a series of amine concentrations and ratios in the formulations were studied using a semibatch bubbling reactor. And due to the formation of ivory-white precipitates in solvents containing higher BZA ratios, a 4:1 molar ratio of MEA/BZA mixed solvent was used to study its performance in a pilot-scale test bed. The results showed that a higher BZA ratio in the MEA/BZA mixed solvent resulted in a faster absorption rate, a higher mass transfer and heat transfer rate and a better cyclic performance, but the mass transfer rate of BZA decreased more quickly than MEA with the increase of CO_2 loading of the solvents. In addition, at high CO_2 loading in the MEA/ BZA mixed solvent with a molar ratio of 4:1, the ivory-white precipitates were generated which could cause blockage of the packing in the absorber, the stripper and the liquid pipelines.
基金The National Natural Science Foundation for Young Scholars of China(No.51106038)the National Key Technology R&D Program of China during the 12th Five-Year Plan Period(No.2012BAA02B01-04)
文摘SO2 release and removal were studied under both the air and oxy-fuel combustion conditions using an anthracite coal from the Jincheng mine in China on a bench-scale fluidized bed combustor （FBC）. Special attention was paid to the effects of the combustion atmosphere, 02 concentration, bed temperature, and limestone addition. The released amount of SO2 was clearly higher under 30% 02/70% CO2 than that of the air atmosphere. As the O2 concentration in O2/CO2 mixture increased from 21% to 40%, the released amount of SO2 increased significantly, but then it decreased when the 02 concentration increased up to 50%. The bed temperature from 860 to 920 ℃ has no obvious influence on the the SO2 release but shows a strong influence on the desulfurization with limestone in both oxy-fuel and air conditions. The maximum SO2 removal efficiency appears to be at 880 to 900 ℃ for both the air and oxy-fuel combustion conditions.
基金Project supported by the National Natural Science Foundation of China (20476002)
文摘The non-grinding long afterglow material SrAl2O4：Eu^2＋ , Dy^3＋ was prepared by combustion method in home mierowave oven direetly, after dispersant, frother, eomburent, and mineralizer were added into the reacting system. XRD analysis showed that the powders were nearly pure SrAl2O4 phase with few other phases, and the size of the grain was 41.1 nm. Fluoreseenee speetrum results indieated that there were 2 exeitation peaks loeated at 345 and 400 nm, and the emission peak loeated at 516 nm, afterglow lasted up to 30 min or more. The mierowave eombustion method has advantages of less time, low temperature and no grinding process, and the material made by the method has good luminescent property.
基金Project(2132046)supported by the Beijing Natural Science Foundation,ChinaProject(51104007)supported by the National Natural Science Foundation of China
文摘Ni-Y2O3 nanocomposite powder with uniform distribution of fine oxide particles in the metal matrix was successfully fabricated via solution combustion process followed by hydrogen reduction. The combustion behavior was investigated by DTA-TG analysis. The influence of urea to nickel nitrate（U/Ni） ratio on the combustion behavior and morphology evolution of the combusted powder was investigated. The morphological characteristics and phase transformation of the combusted powder and the reduced powder were characterized by FESEM, TEM and XRD. The HRTEM image of Ni-Y2O3 nanocomposite powder indicated that Y2O3 particles with average particle size of about 10 nm dispersed uniformly in the nickel matrix.
基金supported by the National High Technology Research and Development Program (863) of China (No.2010AA064904)
文摘Activity and stability of 1%Pd-0.2%Pt/Al2O3 and 1%Pd-0.2%Pt/0.6%Ce/Al2O3 catalysts prepared by impregnation method for catalytic combustion of methane in air were investigated. The catalysts before and after reaction were characterized by BET, CO chemisorption, XRD and XPS techniques. Results showed that the presence of Ce significantly increased the activity and thermal stability of the Pd-Pt/Al2O3 catalyst towards methane combustion, which could be attributed to more highly-dispersed active PdO particles over the Pd-Pt/Ce/Al2O3 catalyst surface as well as the retarded sintering of PdO and the maintained oxidized state of surface Pd during the combustion process in the presence of Ce.
基金supported by the National Natural Science Foundation of China (21273221)the National High Technology Research and Development Program of China (863 Program, 2011AA03A406)
文摘Galvanic deposition method was used to prepare the Pd/Ni-Al2O3-GD catalyst for the combustion of methane under lean conditions. The new catalyst and compared catalysts （Pd/Al2O3-IW, Pd-Ni/Al2O3-IW, Pd/Ni-Al2O3-IW） prepared by incipient wetness impregnation were characterized by N2-physisorption, XRD and TEM to clarify particle size and size distribution of palladium species. Combined O2-TPD and XPS results with the catalytic data, it shows that the surface palladium species with low valence exhibits better combustion performance due to their stronger interaction with support. The results indicate that the galvanic deposition method is an effective route to prepare efficient catalyst for methane combustion, and it also provides useful information for improving the present commercial catalyst.
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...
基金supported by the National Natural Science Foundation of China (60477034)
文摘Blue-green luminescent BaAl2O4：Eu2＋,Dy3＋ phosphor powders were synthesized via combustion synthesis method assisted by microwave irradiation in air. The phosphors were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and fluorescence spectrophotometer. The XRD results revealed that when the concentration of urea was over 3 times higher than theoretical quantities, a BaAl2O4 single hexagonal phase was obtained. The SEM results revealed that the surface of the BaAl2O4：Eu2＋,Dy3＋ powder samples showed lots of voids and pores. The BaAl2O4：Eu2＋,Dy3＋ phosphors exhibited a broad emission band of main peak at 496 nm and a shoulder peak at 426 nm under excitation of 337 nm. The BaAl2O4：Eu2＋,Dy3＋ phosphors at the Eu2＋ concentration of 1 mol.% showed the strongest luminescent intensity. Long afterglow phosphorescence was observed in the dark with naked eyes after the removal of the excitation source.
