A separation method for W and Mo from peroxoacids solution by thermal decomposition wasstudied. Thermal decomposition of peroxotungstic acid and peroxomolybdic acid was investigated respectively. The results confirmed...A separation method for W and Mo from peroxoacids solution by thermal decomposition wasstudied. Thermal decomposition of peroxotungstic acid and peroxomolybdic acid was investigated respectively. The results confirmed that peroxomolybdic acid showed a preferable stability compared with peroxotungstic acid. This thermal stability difference was the basic principle of theseparationof W and Mo. Experiments were performed to study the effects of temperature, stirring speed, free acid concentration and Mo concentration on the separation efficiency. The results indicated that peroxotungstic acid decomposed into tungstic acid（H2WO4） and precipitated selectively,while Mo was rejected in aqueous solution,realizing good separation of W and Mo. The separation factorof W and Moreached 112 under the studied conditions, which indicated that this method has potential for use in separating W and Mo.展开更多
The evolution of a molecular system excited above its ionization threshold depends on a number of parameters that include the nature of the excited states and their couplings to the various continua. The general natur...The evolution of a molecular system excited above its ionization threshold depends on a number of parameters that include the nature of the excited states and their couplings to the various continua. The general nature of the processes governing this evolution depends also essentially on the complexity of the molecule, more precisely on its size, density of states, and strength of the couplings among the various internal degrees of freedom. In this paper we address the question of the transition between autoionization that prevails in small molecules, and delayed ionization occurring in larger molecules or clusters. This transition is illustrated by autoionization of Na2 Rydberg states on one hand, delayed ionization in fullerene C60, and delayed detachment in small cluster anions on the other hand. All processes are studied in the case of nanosecond laser excitation, corresponding to a rather slow deposition of the internal energy.展开更多
The development of bio-based liquid fuel is important for the substitution of transport fuels.Fast pyrolysis can efficiently convert solid biomass wastes into bio-oil.However,its poor properties limit its high-quality...The development of bio-based liquid fuel is important for the substitution of transport fuels.Fast pyrolysis can efficiently convert solid biomass wastes into bio-oil.However,its poor properties limit its high-quality utilization and therefore upgrading is required.Because of the complicated composition,upgrading bio-oil by a single technique faces many problems,such as low conversion efficiency and severe catalyst deactivation.These problems can be largely overcome by graded upgrading based on separation,in which bio-oil is first separated into several fractions and then these fractions are upgraded by different techniques.This paper is a review of the current states in the upgrading of bio-oil fractions obtained from water extraction and vacuum or molecular distillation.The corresponding upgrading techniques include esterification,steam reforming,catalytic cracking,and hydrodeoxygenation. For each upgrading technique,the corresponding conversion behaviors and mechanisms of typical model compounds in bio-oil fractions are first outlined,and then the applications of this technique in actual bio-oil fraction upgrading are introduced.The graded upgrading of bio-oil based on separation will have more potential and become more economical if various separation techniques,upgrading methods,and the extraction of valuable chemicals can be combined.展开更多
An efficient photocatalytic CO_(2) reduction has been reported in ZIF-67-derived-Co nanoparticles(NPs)encapsulated in nitrogen-doped carbon layers(N-C/Co).This work demonstrates that the pyrolysis temperature is cruci...An efficient photocatalytic CO_(2) reduction has been reported in ZIF-67-derived-Co nanoparticles(NPs)encapsulated in nitrogen-doped carbon layers(N-C/Co).This work demonstrates that the pyrolysis temperature is crucial in tuning the grain size and components of metallic Co^(0) of N-C/Co composite catalysts,which optimizes their photocatalytic activities.Syntheses were conducted at 600,700,and 800℃ giving the N-C/Co-600,N-C/Co-700,and N-C/Co-800 samples,respectively.N-C layers can well wrap the Co NPs obtained at a low pyrolysis temperature(600℃)owing to their smaller grains than those of other samples.A high metallic Co^(0) content in the N-C/Co-600 sample can be attributed to the effective inhibition of surface oxidation.By contrast,the surface CoOx oxides in the N-C/Co-700 and N-C/Co-800 samples cover inside Co cores,inhibiting charge separation and transfer.As a result,the N-C/Co-600 sample yields the best photocatalytic activity.The carbon monoxide and hydrogen generation rates are as high as 1.62×10^(4) and 2.01×10^(4)μmol g^(−1)h^(−1),respectively.Additionally,the Co NPs make composite catalysts magnetic,enabling rapid and facile recovery of catalysts with the assistance of an external magnetic field.This work is expected to provide an instructive guideline for designing metal-organic framework-derived carbon/metal composite catalysts.展开更多
The properties of dissolution in different solvents,the specific heat capacity and thermal decomposition process under the non-isothermal conditions for energetic triazole ionic salts 1,2,4-triazolium nitrate(1a),1,2,...The properties of dissolution in different solvents,the specific heat capacity and thermal decomposition process under the non-isothermal conditions for energetic triazole ionic salts 1,2,4-triazolium nitrate(1a),1,2,3-triazolium nitrate(1b),3,4,5triamino-1,2,4-triazolium nitrate(2a),3,4,5-triamino-1,2,4-triazolium dinitramide(2b)were precisely measured using a Calvet Microcalorimeter.The thermochemical equation,differential enthalpies of dissolution(△difH m ),standard molar enthalpies of dissolution(△difH m ),apparent activation energy(E),pre-exponential constant(A),kinetic equation,linear relationship of specific heat capacity with temperature over the temperature range from 283 to 353 K,standard molar heat capacity(C p,m)and enthalpy,entropy and Gibbs free energy at 283–353 K,taking 298.15 K as the benchmark for 1a,1b,2a and 2b were obtained with treating experimental data and theoretical calculation method.The kinetic and thermodynamic parameters of thermal decomposition reaction,critical temperature of thermal explosion(Tb),self-accelerating decomposition temperature(TSADT)and adiabatic time-to-explosion(t)of 1a,1b,2a and 2b were calculated.Their heat-resistance abilities were evaluated.Information was obtained on the relation between molecular structures and properties of 1a,1b,2a and 2b.展开更多
基金Project(51334008)supported by the National Natural Science Foundation of ChinaProject(2010FJ1011)supported by the Key Program of Science and Technology of Hunan Province,China
文摘A separation method for W and Mo from peroxoacids solution by thermal decomposition wasstudied. Thermal decomposition of peroxotungstic acid and peroxomolybdic acid was investigated respectively. The results confirmed that peroxomolybdic acid showed a preferable stability compared with peroxotungstic acid. This thermal stability difference was the basic principle of theseparationof W and Mo. Experiments were performed to study the effects of temperature, stirring speed, free acid concentration and Mo concentration on the separation efficiency. The results indicated that peroxotungstic acid decomposed into tungstic acid（H2WO4） and precipitated selectively,while Mo was rejected in aqueous solution,realizing good separation of W and Mo. The separation factorof W and Moreached 112 under the studied conditions, which indicated that this method has potential for use in separating W and Mo.
文摘The evolution of a molecular system excited above its ionization threshold depends on a number of parameters that include the nature of the excited states and their couplings to the various continua. The general nature of the processes governing this evolution depends also essentially on the complexity of the molecule, more precisely on its size, density of states, and strength of the couplings among the various internal degrees of freedom. In this paper we address the question of the transition between autoionization that prevails in small molecules, and delayed ionization occurring in larger molecules or clusters. This transition is illustrated by autoionization of Na2 Rydberg states on one hand, delayed ionization in fullerene C60, and delayed detachment in small cluster anions on the other hand. All processes are studied in the case of nanosecond laser excitation, corresponding to a rather slow deposition of the internal energy.
基金financial support from the National Natural Science Foundation of China(Grant Nos.50676085,51276166,50476057,50176046 and 51476142)
文摘The development of bio-based liquid fuel is important for the substitution of transport fuels.Fast pyrolysis can efficiently convert solid biomass wastes into bio-oil.However,its poor properties limit its high-quality utilization and therefore upgrading is required.Because of the complicated composition,upgrading bio-oil by a single technique faces many problems,such as low conversion efficiency and severe catalyst deactivation.These problems can be largely overcome by graded upgrading based on separation,in which bio-oil is first separated into several fractions and then these fractions are upgraded by different techniques.This paper is a review of the current states in the upgrading of bio-oil fractions obtained from water extraction and vacuum or molecular distillation.The corresponding upgrading techniques include esterification,steam reforming,catalytic cracking,and hydrodeoxygenation. For each upgrading technique,the corresponding conversion behaviors and mechanisms of typical model compounds in bio-oil fractions are first outlined,and then the applications of this technique in actual bio-oil fraction upgrading are introduced.The graded upgrading of bio-oil based on separation will have more potential and become more economical if various separation techniques,upgrading methods,and the extraction of valuable chemicals can be combined.
基金financially supported by the National Key Research and Development Program of China(2020YFA0710303)the National Natural Science Foundation of China(51972061,U1905215 and 52072076)。
文摘An efficient photocatalytic CO_(2) reduction has been reported in ZIF-67-derived-Co nanoparticles(NPs)encapsulated in nitrogen-doped carbon layers(N-C/Co).This work demonstrates that the pyrolysis temperature is crucial in tuning the grain size and components of metallic Co^(0) of N-C/Co composite catalysts,which optimizes their photocatalytic activities.Syntheses were conducted at 600,700,and 800℃ giving the N-C/Co-600,N-C/Co-700,and N-C/Co-800 samples,respectively.N-C layers can well wrap the Co NPs obtained at a low pyrolysis temperature(600℃)owing to their smaller grains than those of other samples.A high metallic Co^(0) content in the N-C/Co-600 sample can be attributed to the effective inhibition of surface oxidation.By contrast,the surface CoOx oxides in the N-C/Co-700 and N-C/Co-800 samples cover inside Co cores,inhibiting charge separation and transfer.As a result,the N-C/Co-600 sample yields the best photocatalytic activity.The carbon monoxide and hydrogen generation rates are as high as 1.62×10^(4) and 2.01×10^(4)μmol g^(−1)h^(−1),respectively.Additionally,the Co NPs make composite catalysts magnetic,enabling rapid and facile recovery of catalysts with the assistance of an external magnetic field.This work is expected to provide an instructive guideline for designing metal-organic framework-derived carbon/metal composite catalysts.
基金supported by the National Natural Science Foundation of China (20573098)the Science and Technology Foundation of National Key Lab of Science and Technology on Combustion and Explosion in China (9140C3503030805)
文摘The properties of dissolution in different solvents,the specific heat capacity and thermal decomposition process under the non-isothermal conditions for energetic triazole ionic salts 1,2,4-triazolium nitrate(1a),1,2,3-triazolium nitrate(1b),3,4,5triamino-1,2,4-triazolium nitrate(2a),3,4,5-triamino-1,2,4-triazolium dinitramide(2b)were precisely measured using a Calvet Microcalorimeter.The thermochemical equation,differential enthalpies of dissolution(△difH m ),standard molar enthalpies of dissolution(△difH m ),apparent activation energy(E),pre-exponential constant(A),kinetic equation,linear relationship of specific heat capacity with temperature over the temperature range from 283 to 353 K,standard molar heat capacity(C p,m)and enthalpy,entropy and Gibbs free energy at 283–353 K,taking 298.15 K as the benchmark for 1a,1b,2a and 2b were obtained with treating experimental data and theoretical calculation method.The kinetic and thermodynamic parameters of thermal decomposition reaction,critical temperature of thermal explosion(Tb),self-accelerating decomposition temperature(TSADT)and adiabatic time-to-explosion(t)of 1a,1b,2a and 2b were calculated.Their heat-resistance abilities were evaluated.Information was obtained on the relation between molecular structures and properties of 1a,1b,2a and 2b.
