An intrinsic kinetics of cyclohexanone ammoximation in the liquid phase over titanium silicate molecular sieves is investigated in an isothermal slurry reactor at different initial reactant concentrations, catalyst lo...An intrinsic kinetics of cyclohexanone ammoximation in the liquid phase over titanium silicate molecular sieves is investigated in an isothermal slurry reactor at different initial reactant concentrations, catalyst loading, and reaction temperature. The rate equations are developed by analyzing data of kinetic measurements. More than 10 side reactions were found. H2O2 decomposition reaction must be considered and other side reactions can be neglected in the kinetic modeling. The predicted values of reaction rates based on the kinetic models are almost consistent with experimental ones. The models have guidance to the selection of reactor types and they are useful to the design and operation of reactor used.展开更多
Alkali halides crystals have been the subject of intense research. High order crystalline one phase mixtures （high order： more that binary） studied by TL （thermoluminiscence technique） proved having persistent pe...Alkali halides crystals have been the subject of intense research. High order crystalline one phase mixtures （high order： more that binary） studied by TL （thermoluminiscence technique） proved having persistent peaks along the time after the radiation to which they are exposed. In general in alkali halide crystals the traps associated with highest recorded temperature peaks in the TL due to radiation damage have greater permanence in time too. These features are useful for dosimetric applications. In this work, temperature thermoluminescence glow peaks of ternary and quaternary mixed alkali halide crystals have been studied. The study has been focused on their high temperature glow peaks after being subjected to thermal treatments at 373, 573, and 673 K. The glow peaks of high temperature were isolated and studied 24 h and 48 h after irradiation. The parameters of the recombination processes associated to these peaks were obtained using a glow peak shape method. Orders of kinetics were higher than 1.0 and the activation energy greater than 1.2 eV. The results suggest that such materials have a high potential as dosimeter and energy storage materials.展开更多
The selective hydrogenation of halogenated nitrobenzene over noble metal catalysts(Pd, Pt, and Ir) has attracted much attention owing to its high efficiency and environmental friendliness. However, the effect of size ...The selective hydrogenation of halogenated nitrobenzene over noble metal catalysts(Pd, Pt, and Ir) has attracted much attention owing to its high efficiency and environmental friendliness. However, the effect of size on the catalytic performance varies among different metal catalysts. In this study, sub-nano(<3 nm) Ir and Pd particles were prepared, and their catalytic properties for hydrogenation of halogenated nitrobenzene were evaluated.Results show that high selectivity(N 99%) was achieved over small Ir nanoparticles, in which the selectivity over the Pd with same size was much lower than that on Ir nanoparticles. Meanwhile, Ir and Pd have different hydrogen consumption rates and reaction rates. Density functional theory calculations showed that p-chloronitrobenzene(CNB) has different adsorption properties on Ir and Pd. The distance between oxygen(cholorine) and Ir is much shorter(longer) than that between oxygen and Pd. The reaction barriers of dechlorination of p-CNB and p-chloroaniline over different Ir models are much larger than those on Pd. Especially,lower coordination of Ir leads to larger barriers of dechlorination reaction. These theoretical results explain the difference between Ir and Pd on hydrogenation of halogenated nitrobenzene.展开更多
Rubidium phosphate can be more conveniently obtained by extracting trace Rb+ from the salt lake brine. Rb_3PO_4 was found to be an excellent heterogeneous catalyst for transfer hydrogenation. Rb_3PO_4 lost 70% of its ...Rubidium phosphate can be more conveniently obtained by extracting trace Rb+ from the salt lake brine. Rb_3PO_4 was found to be an excellent heterogeneous catalyst for transfer hydrogenation. Rb_3PO_4 lost 70% of its active sites after adsorbing water, but the remaining was not affected. The reductions of aldehydes and ketones, when promoted by Rb_3PO_4, were allowed at room temperature. The activities of substrates at room temperature followed a descending order of 2,6-dichlorobenzaldehyde> 4-bromobenzaldehyde>benzaldehyde>acetophenone>anisaldehyde>butanone. A new catalytic cycle postulating a six-membered cyclic transition state for the reductions of aldehydes and ketones was proposed. These results exploited the catalytic usage of Rb_3PO_4 and worth in industrial application.展开更多
Synthesis of organosilanes from alkenes is a very important topic owing to their wide applications.A Ni/Cu dual metal-catalyzed arylsilylation of terminal alkenes,featuring migratory selectivity,has been developed.A w...Synthesis of organosilanes from alkenes is a very important topic owing to their wide applications.A Ni/Cu dual metal-catalyzed arylsilylation of terminal alkenes,featuring migratory selectivity,has been developed.A wide diversity of aliphatic silanes have been prepared from terminal alkenes,aryl halides and Suginome’s reagent.This protocol is highlighted by excellent regioselectivity,mild reaction conditions and good functional group tolerance.In addition to benzylic positions,carbon–carbon bonds can also be constructed at allylic positions.Preliminary mechanistic studies suggest that the copper cocatalyst promotes the transmetalation of Suginome’s reagent,and the addition of a Pyr Ox ligand inhibits the formation of side-products from the carbon-Heck pathway.Moreover,studies toward the nature of the Pyr Ox ligand revealed that the steric hindrance of the oxazoline moiety greatly affects the chain–walking process,but not the arylation step.展开更多
Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved,providing a new,simple,and efficient method for conducting highly regioselective hydrodehalogenation.This method not only features ...Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved,providing a new,simple,and efficient method for conducting highly regioselective hydrodehalogenation.This method not only features a readily available reductant,an inexpensive catalyst,simple manipulation,and good tolerance of functional groups including nitriles,nitro,esters,and methoxyl groups,it also has mild reaction conditions and shows complete regioselectivity in that only halides sited at the allylic position are reduced.Alternatively,this method can be applied in the selective transformation of benzylic alcohols to aromatic aldehydes without overoxidation to carboxylic acids.展开更多
Monodisperse Pt nanoparticles(NPs) were prepared by reduction of platinum acetylacetonate in octadecene with the presence of Fe(CO)5. The synthesized nanocatalysts presented high activity and selectively for hydrogena...Monodisperse Pt nanoparticles(NPs) were prepared by reduction of platinum acetylacetonate in octadecene with the presence of Fe(CO)5. The synthesized nanocatalysts presented high activity and selectively for hydrogenation of ortho-halogenated nitrobenzene to the corresponding ortho-halogenated aniline under mild reaction conditions.展开更多
文摘An intrinsic kinetics of cyclohexanone ammoximation in the liquid phase over titanium silicate molecular sieves is investigated in an isothermal slurry reactor at different initial reactant concentrations, catalyst loading, and reaction temperature. The rate equations are developed by analyzing data of kinetic measurements. More than 10 side reactions were found. H2O2 decomposition reaction must be considered and other side reactions can be neglected in the kinetic modeling. The predicted values of reaction rates based on the kinetic models are almost consistent with experimental ones. The models have guidance to the selection of reactor types and they are useful to the design and operation of reactor used.
文摘Alkali halides crystals have been the subject of intense research. High order crystalline one phase mixtures （high order： more that binary） studied by TL （thermoluminiscence technique） proved having persistent peaks along the time after the radiation to which they are exposed. In general in alkali halide crystals the traps associated with highest recorded temperature peaks in the TL due to radiation damage have greater permanence in time too. These features are useful for dosimetric applications. In this work, temperature thermoluminescence glow peaks of ternary and quaternary mixed alkali halide crystals have been studied. The study has been focused on their high temperature glow peaks after being subjected to thermal treatments at 373, 573, and 673 K. The glow peaks of high temperature were isolated and studied 24 h and 48 h after irradiation. The parameters of the recombination processes associated to these peaks were obtained using a glow peak shape method. Orders of kinetics were higher than 1.0 and the activation energy greater than 1.2 eV. The results suggest that such materials have a high potential as dosimeter and energy storage materials.
基金Supported by the National Natural Science Foundation of China(Nos.21473159 and91334013)
文摘The selective hydrogenation of halogenated nitrobenzene over noble metal catalysts(Pd, Pt, and Ir) has attracted much attention owing to its high efficiency and environmental friendliness. However, the effect of size on the catalytic performance varies among different metal catalysts. In this study, sub-nano(<3 nm) Ir and Pd particles were prepared, and their catalytic properties for hydrogenation of halogenated nitrobenzene were evaluated.Results show that high selectivity(N 99%) was achieved over small Ir nanoparticles, in which the selectivity over the Pd with same size was much lower than that on Ir nanoparticles. Meanwhile, Ir and Pd have different hydrogen consumption rates and reaction rates. Density functional theory calculations showed that p-chloronitrobenzene(CNB) has different adsorption properties on Ir and Pd. The distance between oxygen(cholorine) and Ir is much shorter(longer) than that between oxygen and Pd. The reaction barriers of dechlorination of p-CNB and p-chloroaniline over different Ir models are much larger than those on Pd. Especially,lower coordination of Ir leads to larger barriers of dechlorination reaction. These theoretical results explain the difference between Ir and Pd on hydrogenation of halogenated nitrobenzene.
基金Project(21576074)supported by the National Natural Science Foundation of China
文摘Rubidium phosphate can be more conveniently obtained by extracting trace Rb+ from the salt lake brine. Rb_3PO_4 was found to be an excellent heterogeneous catalyst for transfer hydrogenation. Rb_3PO_4 lost 70% of its active sites after adsorbing water, but the remaining was not affected. The reductions of aldehydes and ketones, when promoted by Rb_3PO_4, were allowed at room temperature. The activities of substrates at room temperature followed a descending order of 2,6-dichlorobenzaldehyde> 4-bromobenzaldehyde>benzaldehyde>acetophenone>anisaldehyde>butanone. A new catalytic cycle postulating a six-membered cyclic transition state for the reductions of aldehydes and ketones was proposed. These results exploited the catalytic usage of Rb_3PO_4 and worth in industrial application.
基金supported by the National Natural Science Foundation of China(21702151,21774029,and 21871211)the Fundamental Research Funds for Central Universities(2042019kf0208)。
文摘Synthesis of organosilanes from alkenes is a very important topic owing to their wide applications.A Ni/Cu dual metal-catalyzed arylsilylation of terminal alkenes,featuring migratory selectivity,has been developed.A wide diversity of aliphatic silanes have been prepared from terminal alkenes,aryl halides and Suginome’s reagent.This protocol is highlighted by excellent regioselectivity,mild reaction conditions and good functional group tolerance.In addition to benzylic positions,carbon–carbon bonds can also be constructed at allylic positions.Preliminary mechanistic studies suggest that the copper cocatalyst promotes the transmetalation of Suginome’s reagent,and the addition of a Pyr Ox ligand inhibits the formation of side-products from the carbon-Heck pathway.Moreover,studies toward the nature of the Pyr Ox ligand revealed that the steric hindrance of the oxazoline moiety greatly affects the chain–walking process,but not the arylation step.
基金the National Natural Science Foundation of China(21132002&21272038)the National Basic Research Programm of China(973 program,2009CB825300)the Shanghai Leading Academic Discipline Project(B108)for financial support
文摘Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved,providing a new,simple,and efficient method for conducting highly regioselective hydrodehalogenation.This method not only features a readily available reductant,an inexpensive catalyst,simple manipulation,and good tolerance of functional groups including nitriles,nitro,esters,and methoxyl groups,it also has mild reaction conditions and shows complete regioselectivity in that only halides sited at the allylic position are reduced.Alternatively,this method can be applied in the selective transformation of benzylic alcohols to aromatic aldehydes without overoxidation to carboxylic acids.
基金financially supported by the National Natural Science Foundation of China(21373006,51402203)the Natural Science Foundation of Jiangsu Province for Young Scholars(BK20140326)+1 种基金the Natural Science Foundation of Jiangsu Higher Education Institutions(14KJB430021)the Priority Academic Program Development of Jiangsu Higher Education Institutions
文摘Monodisperse Pt nanoparticles(NPs) were prepared by reduction of platinum acetylacetonate in octadecene with the presence of Fe(CO)5. The synthesized nanocatalysts presented high activity and selectively for hydrogenation of ortho-halogenated nitrobenzene to the corresponding ortho-halogenated aniline under mild reaction conditions.
