Catalytic hydrogenation of CO_(2) using renewable hydrogen not only reduces greenhouse gas emissions,but also provides industrial chemicals.Herein,a Co-Fe bimetallic catalyst was developed by a facile reactive ball-mi...Catalytic hydrogenation of CO_(2) using renewable hydrogen not only reduces greenhouse gas emissions,but also provides industrial chemicals.Herein,a Co-Fe bimetallic catalyst was developed by a facile reactive ball-milling method for highly active and selective hydrogenation of CO_(2) to value-added hydrocarbons.When reacted at 320℃,1.0 MPa and 9600 mL h^(-1) g_(cat)^(-1),the selectivity to light olefin(C_(2)^(=)-C_(4)^(=)) and C_(5)+ species achieves 57.3% and 22.3%,respectively,at a CO_(2) co nversion of 31.4%,which is superior to previous Fe-based catalysts.The CO_(2) activation can be promoted by the CoFe phase formed by reactive ball milling of the Fe-Co_(3)O_(4) mixture,and the in-situ Co_(2)C and Fe_(5)C_(2) formed during hydrogenation are beneficial for the C-C coupling reaction.The initial C-C coupling is related to the combination of CO species with the surface carbon of Fe/Co carbides,and the sustained C-C coupling is maintained by self-recovery of defective carbides.This new strategy contributes to the development of efficient catalysts for the hydrogenation of CO_(2) to value-added hydrocarbons.展开更多
A TiAl alloy was fabricated by high-energy ball milling and subsequent reactive sintering from the mixed powders of Ti and Al. High-energy ball milling produced a kind of particular composite powders with an extremely...A TiAl alloy was fabricated by high-energy ball milling and subsequent reactive sintering from the mixed powders of Ti and Al. High-energy ball milling produced a kind of particular composite powders with an extremely fine altemative Ti and Al lamella structure. The composite powders not only possessed good consolidation and densification characteristics, but also resulted in the augment of nucleation rate of α and γ titanium aluminides during solid-phase reactive sintering After a series of processing, pressing, degassing, extrusion, and sintering, the resultant TiAl alloy presented high relative density and refined grain sizes of （α2 ＋ γ） lamella and γ phases. The compressive yield strength of the sintered TiAl reached 600 MPa at 800℃.展开更多
Li-Mg-N-B-H/ZrCoH_(3) composites were successfully synthesized by ball milling of the reactants under argon and hydrogen atmosphere,respectively.The composite synthesized by reactive ball milling(RBM)under hydrogen ha...Li-Mg-N-B-H/ZrCoH_(3) composites were successfully synthesized by ball milling of the reactants under argon and hydrogen atmosphere,respectively.The composite synthesized by reactive ball milling(RBM)under hydrogen has the best hydrogen storage properties.It can desorb 3.71 wt%hydrogen in 60 min at 150℃under pressure of 0.1 MPa,and the dehydrogenation capacity reaches 4.59 wt%in 8 h.For the re-hydrogenation,5.27 wt%hydrogen was absorbed in only 10 min at 150℃under H_(2) pressure of 8 MPa.The phases of the as-milled and subsequently dehydrogenated and re-hydrogenated samples were determined by X-ray diffraction(XRD).The microstructures and elemental distributions were characterized by scanning electron microscope(SEM)and energy-dispersive spectrometer(EDS)measurements.It is shown that Mg is in situ hydrogenated and introduced homogeneous distribution of ZrCoH_(3) particles during the RBM process under hydrogen atmosphere.The activation energies for the composites were calculated by Kissinger method through differential scanning calorimetric(DSC)measurements for the dehydrogenation process with different heating rates.It is determined that the activation energy for the Li-Mg-N-B-H/ZrCoH_(3) composite synthesized by RBM under hydrogen is 79.9 kJ·mol^(-1),which is14 kJ·mol^(-1) lower than that for the sample without ZrCoH_(3) addition.The N-H bond energies were analyzed by infrared(IR)absorption spectrum,and the reasons for weakening of the N-H bond were further discussed.展开更多
In this paper,various core-shell structured Al—Ni@ECs composites have been prepared by a spray-drying technique.The involved ECs refer to the energetic composites(ECs)of ammonium perchlorate/nitrocellulose(AP/NC,NA)a...In this paper,various core-shell structured Al—Ni@ECs composites have been prepared by a spray-drying technique.The involved ECs refer to the energetic composites(ECs)of ammonium perchlorate/nitrocellulose(AP/NC,NA)and polyvinylidene fluoride/hexanitrohexaazaisowurtzitane(PVDF/CL-20,PC).Two Al—Ni mixtures were prepared at atomic ratios of 1:1 and 1:3 and named as Al/Ni and Al/3Ni,respectively.The thermal reactivity and combustion behaviors of Al—Ni@ECs composites have been comprehensively investigated.Results showed that the reactivity and combustion performance of Al—Ni could be enhanced by introducing both NA and PC energetic composites.Among which the Al/Ni@NA composite exhibited higher reactivity and improved combustion performance.The measured flame propagation rate(v=20.6 mm/s),average combustion wave temperature(T_(max)=1567.0°C)and maximum temperature rise rate(γ_(t)=1633.6°C/s)of Al/Ni@NA are higher than that of the Al/Ni(v=15.8 mm/s,T_(max)=858.0°C,andγ_(t)=143.5°C/s).The enhancement in combustion properties could be due to presence of the acidic gaseous products from ECs,which could etch the Al_(2)O_(3)shell on the surface of Al particles,and make the inner active Al to be easier transported,so that an intimate and faster intermetallic reaction between Al and Ni would be realized.Furthermore,the morphologies and chemical compositions of the condensed combustion products(CCPs)of Al—Ni@ECs composites were found to be different depending on the types of ECs.The compositions of CCPs are dominated with the Al—Ni intermetallics,combining with a trace amount of Al_(5)O_(6)N and Al_(2)O_(3).展开更多
为提高铝粉与海水的反应效率和速率,在惰性氛围下,采用高能球磨法通过多次变速循环工艺制备得到了铝基水反应活性材料。通过扫描电子显微镜、热重分析仪、比表面测试等分析表征材料的微观结构和氧化性能;采用自主设计的金属/水反应装置...为提高铝粉与海水的反应效率和速率,在惰性氛围下,采用高能球磨法通过多次变速循环工艺制备得到了铝基水反应活性材料。通过扫描电子显微镜、热重分析仪、比表面测试等分析表征材料的微观结构和氧化性能;采用自主设计的金属/水反应装置,实时记录铝基水反应金属材料与海水反应产生的氢气量,研究铝基水反应活性材料的活性。研究结果表明:高能球磨能提高铝基材料与海水的反应活性,铝粉经过球磨后反应效率达到原先的2倍;球磨过程中添加剂铋的添加能进一步提高铝基水反应材料的活性;反应总产率能够达到71.2%,其快速期氢气产生反应速率为210.7 m L/(min·g)。制备的铝基水反应活性材料在高能水反应金属燃料推进剂和制氢领域都具有应用价值。展开更多
基金supported by the National Natural Science Foundation of China (22008098, 21978156, 42002040)the Program for Innovative Research Team (in Science and Technology) in University of Henan Province (21IRTSTHN004)+1 种基金the Program for Science & Technology Innovation Talents in Universities of Henan Province (22HASTIT008)the Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering (2022-K34)。
文摘Catalytic hydrogenation of CO_(2) using renewable hydrogen not only reduces greenhouse gas emissions,but also provides industrial chemicals.Herein,a Co-Fe bimetallic catalyst was developed by a facile reactive ball-milling method for highly active and selective hydrogenation of CO_(2) to value-added hydrocarbons.When reacted at 320℃,1.0 MPa and 9600 mL h^(-1) g_(cat)^(-1),the selectivity to light olefin(C_(2)^(=)-C_(4)^(=)) and C_(5)+ species achieves 57.3% and 22.3%,respectively,at a CO_(2) co nversion of 31.4%,which is superior to previous Fe-based catalysts.The CO_(2) activation can be promoted by the CoFe phase formed by reactive ball milling of the Fe-Co_(3)O_(4) mixture,and the in-situ Co_(2)C and Fe_(5)C_(2) formed during hydrogenation are beneficial for the C-C coupling reaction.The initial C-C coupling is related to the combination of CO species with the surface carbon of Fe/Co carbides,and the sustained C-C coupling is maintained by self-recovery of defective carbides.This new strategy contributes to the development of efficient catalysts for the hydrogenation of CO_(2) to value-added hydrocarbons.
基金This project was financially supported by the National Natural Science Foundation of China (No. 59875015)the Natural Science Foundation of South China University of Technology (No. E5305293).
文摘A TiAl alloy was fabricated by high-energy ball milling and subsequent reactive sintering from the mixed powders of Ti and Al. High-energy ball milling produced a kind of particular composite powders with an extremely fine altemative Ti and Al lamella structure. The composite powders not only possessed good consolidation and densification characteristics, but also resulted in the augment of nucleation rate of α and γ titanium aluminides during solid-phase reactive sintering After a series of processing, pressing, degassing, extrusion, and sintering, the resultant TiAl alloy presented high relative density and refined grain sizes of （α2 ＋ γ） lamella and γ phases. The compressive yield strength of the sintered TiAl reached 600 MPa at 800℃.
基金financially supported by Beijing Science and Technology Program(No.D141100002014002)。
文摘Li-Mg-N-B-H/ZrCoH_(3) composites were successfully synthesized by ball milling of the reactants under argon and hydrogen atmosphere,respectively.The composite synthesized by reactive ball milling(RBM)under hydrogen has the best hydrogen storage properties.It can desorb 3.71 wt%hydrogen in 60 min at 150℃under pressure of 0.1 MPa,and the dehydrogenation capacity reaches 4.59 wt%in 8 h.For the re-hydrogenation,5.27 wt%hydrogen was absorbed in only 10 min at 150℃under H_(2) pressure of 8 MPa.The phases of the as-milled and subsequently dehydrogenated and re-hydrogenated samples were determined by X-ray diffraction(XRD).The microstructures and elemental distributions were characterized by scanning electron microscope(SEM)and energy-dispersive spectrometer(EDS)measurements.It is shown that Mg is in situ hydrogenated and introduced homogeneous distribution of ZrCoH_(3) particles during the RBM process under hydrogen atmosphere.The activation energies for the composites were calculated by Kissinger method through differential scanning calorimetric(DSC)measurements for the dehydrogenation process with different heating rates.It is determined that the activation energy for the Li-Mg-N-B-H/ZrCoH_(3) composite synthesized by RBM under hydrogen is 79.9 kJ·mol^(-1),which is14 kJ·mol^(-1) lower than that for the sample without ZrCoH_(3) addition.The N-H bond energies were analyzed by infrared(IR)absorption spectrum,and the reasons for weakening of the N-H bond were further discussed.
基金supported by the Nation Natural Science Foundation of China(Grant No.51776176)the Fundamental Research Funds for the Central Universities,China(Grant No.G2017KY0301)+1 种基金partially funded by NSAF project(Grant No.2030202)sponsored by Innovation Foundation for Doctor Dissertation of Northwestern Polytechnical University(Grant No.CX2021048)。
文摘In this paper,various core-shell structured Al—Ni@ECs composites have been prepared by a spray-drying technique.The involved ECs refer to the energetic composites(ECs)of ammonium perchlorate/nitrocellulose(AP/NC,NA)and polyvinylidene fluoride/hexanitrohexaazaisowurtzitane(PVDF/CL-20,PC).Two Al—Ni mixtures were prepared at atomic ratios of 1:1 and 1:3 and named as Al/Ni and Al/3Ni,respectively.The thermal reactivity and combustion behaviors of Al—Ni@ECs composites have been comprehensively investigated.Results showed that the reactivity and combustion performance of Al—Ni could be enhanced by introducing both NA and PC energetic composites.Among which the Al/Ni@NA composite exhibited higher reactivity and improved combustion performance.The measured flame propagation rate(v=20.6 mm/s),average combustion wave temperature(T_(max)=1567.0°C)and maximum temperature rise rate(γ_(t)=1633.6°C/s)of Al/Ni@NA are higher than that of the Al/Ni(v=15.8 mm/s,T_(max)=858.0°C,andγ_(t)=143.5°C/s).The enhancement in combustion properties could be due to presence of the acidic gaseous products from ECs,which could etch the Al_(2)O_(3)shell on the surface of Al particles,and make the inner active Al to be easier transported,so that an intimate and faster intermetallic reaction between Al and Ni would be realized.Furthermore,the morphologies and chemical compositions of the condensed combustion products(CCPs)of Al—Ni@ECs composites were found to be different depending on the types of ECs.The compositions of CCPs are dominated with the Al—Ni intermetallics,combining with a trace amount of Al_(5)O_(6)N and Al_(2)O_(3).
文摘为提高铝粉与海水的反应效率和速率,在惰性氛围下,采用高能球磨法通过多次变速循环工艺制备得到了铝基水反应活性材料。通过扫描电子显微镜、热重分析仪、比表面测试等分析表征材料的微观结构和氧化性能;采用自主设计的金属/水反应装置,实时记录铝基水反应金属材料与海水反应产生的氢气量,研究铝基水反应活性材料的活性。研究结果表明:高能球磨能提高铝基材料与海水的反应活性,铝粉经过球磨后反应效率达到原先的2倍;球磨过程中添加剂铋的添加能进一步提高铝基水反应材料的活性;反应总产率能够达到71.2%,其快速期氢气产生反应速率为210.7 m L/(min·g)。制备的铝基水反应活性材料在高能水反应金属燃料推进剂和制氢领域都具有应用价值。
