An efficient and environmentally friendly procedure was described for easy product isolation for the oxidation of cyclohexane with tert-butyl-hydroperoxide catalyzed by titanium silicalite 1 （TS-1） in ambient-temper...An efficient and environmentally friendly procedure was described for easy product isolation for the oxidation of cyclohexane with tert-butyl-hydroperoxide catalyzed by titanium silicalite 1 （TS-1） in ambient-temperature ionic liquid [emim]BF4. Good yield and higher selectivity of products were found in the ionic liquid compared with in molecular solvent. The research results showed 13.2% conversion of cyclohexane, 97.6% cyclohexanol and cyclohexanone selectivity were obtained in ionic liquid under mild conditions of 90℃.展开更多
Au-Ag bimetallic nanoparticle‐supported microporous titanium silicalite‐1catalysts were prepared via a hydrothermal‐immersion method,and their structures were examined.These materials serve as efficient catalysts f...Au-Ag bimetallic nanoparticle‐supported microporous titanium silicalite‐1catalysts were prepared via a hydrothermal‐immersion method,and their structures were examined.These materials serve as efficient catalysts for the photosynthesis of propylene oxide via the epoxidation of propene.The Au/Ag mass ratio and reaction temperature were demonstrated to have significant effects on the catalytic activity and selectivity of propylene oxide.The optimal formation rate(68.3μmol/g·h)and selectivity(52.3%)toward propylene oxide were achieved with an Au:Ag mass ratio of4:1.Notably,the strong synergistic effect between Au and Ag resulted in superior photocatalysis of the bimetallic systems compared with those of the individual systems.A probable reaction mechanism was proposed based on the theoretical and experimental results.展开更多
Selective and durable fixed‐bed catalysts are highly desirable for developing eco‐efficient HPPO(hydrogen peroxide propylene oxide)process.The powder titanosilicate catalysts must be shaped before being applied in i...Selective and durable fixed‐bed catalysts are highly desirable for developing eco‐efficient HPPO(hydrogen peroxide propylene oxide)process.The powder titanosilicate catalysts must be shaped before being applied in industrial processes.As the essential additives for preparing formed catalysts,binders are usually the catalytically inert components,but they would cover the surface and pore mouth of zeolite,thereby declining the accessibility of active sites.By recrystallizing the binder(silica)/Ti‐MWW extrudates with the assistance of dual organic structure‐directing agents,the silica binder was converted into MWW zeolite phase to form a structured binder‐free Ti‐MWW zeolite with Si‐rich shell,which enhanced the diffusion efficiency and maintained the mechanical strength.Meanwhile,due to the partial dissolution of Si in the Ti‐MWW matrix,abundant silanol nests formed and part of framework TiO4 species were transferred into open TiO_(6)ones,improving the accumulation and activation ability of H_(2)O_(2)inside the monolith.Successive piperidine treatment and fluoridation of the binder‐free Ti‐MWW further enhanced the H_(2)O_(2)activation and oxygen transfer ability of the active Ti sites,and stabilized the Ti‐OOH intermediate through hydrogen bond formed between the end H in Ti‐OOH and the adjacent Si‐F species,thus achieving a more efficient epoxidation process.Additionally,the side reaction of PO hydrolysis was inhibited because the modification effectively quenched numerous Si‐OH groups.The lifetime of the modified binder‐free Ti‐MWW catalyst was 2400 h with the H_(2)O_(2)conversion and PO selectivity both above 99.5%.展开更多
Hollow titanium silicalite （HTS） molecular sieve has been synthesized, and information on its structure, physico- chemical characterization, as well as surface property was investigated by a host of analytical metho...Hollow titanium silicalite （HTS） molecular sieve has been synthesized, and information on its structure, physico- chemical characterization, as well as surface property was investigated by a host of analytical methods, such as XRF, XRD, low-temperature N2 adsorption/desorption, TEM, FT-IR, UV-Vis, 29Si MAS NIVIR, and XPS techniques. The characterization results suggest that HTS zeolite has a special hollow crystal structure and its mesopore volume is larger than that of TS-1 zeolite. The titanium species in this zeolite are composed of the framework tetrahedral Ti （IV） ions and extra-framework octahedral Ti （IV） ions, which tend to disperse into its bulk phase. This zeolite material also has been applied to catalyze the cyclohexanone oxidation process, and the products are not completely consistent with those results obtained by using TS-1 zeolite, which might be caused by their difference in pore structure and pore volume, especially the mesopore volume. Cy- clohexanone oxidation catalyzed by HTS zeolite is a representative consecutive reaction, the main target products of which are e-caprolactone, 6-hydroxyhexanoic acid and adipic acid. The effect of H202/cyclohexanone mole ratio on the cyclohexa- none conversion, the total target product selectivity, the distribution of three target products selectivity and their variations along with reaction time is also researched and analyzed, which indicate that HTS zeolite shows a high performance for the Baeyer-Villiger reaction of cyclohexanone and catalytic oxidation of 6-hydroxyhexanoic acid under mild conditions, and the quantity of active surface titanium species as well as the pore structure and mesopore volume controlling the mass diffusion rate are the key factors determining the catalytic activity of HTS zeolite and product selectivity.展开更多
29Si-NMR and 1H-NMR were used to follow up the basic hydrolysis of tetraethyl orthosilicate （TOES） and the results showed that species of monomer, dimer, trimer, cyclic and polymer silicates were formed. The monomer...29Si-NMR and 1H-NMR were used to follow up the basic hydrolysis of tetraethyl orthosilicate （TOES） and the results showed that species of monomer, dimer, trimer, cyclic and polymer silicates were formed. The monomer and dimer were favorable for the high activity of zeolite. XRD, 13C CP/MAS and 29Si NMR were used to trace the crystallization process of hollow titanium silicalite zeolites （HTS）. The results showed that the induction period of HTS was 80 min, and subsequently it took next 10 min to form HTS and the remaining time of the crystallization period might function for cleaning up the pores and/or washing off the impurities from the HTS zeolite. The catalytic oxidation performance of HTS zeolite is different from that of the acid activity of zeolite in which the conventional definition of crystallinity does not reflect the catalytic oxidation activity proportionally. The synthesized HTS samples were character- ized by XRD, FT-IR, UV-Vis and Raman spectra. It was confirmed that Ti was incorporated into the zeolite framework. The synthesized HTS samples revealed good repeatability and high activity for oxidation of phenol into diphenol.展开更多
基金Supported by the National Natural Science Foundation of China （20776037）.
文摘An efficient and environmentally friendly procedure was described for easy product isolation for the oxidation of cyclohexane with tert-butyl-hydroperoxide catalyzed by titanium silicalite 1 （TS-1） in ambient-temperature ionic liquid [emim]BF4. Good yield and higher selectivity of products were found in the ionic liquid compared with in molecular solvent. The research results showed 13.2% conversion of cyclohexane, 97.6% cyclohexanol and cyclohexanone selectivity were obtained in ionic liquid under mild conditions of 90℃.
基金supported by the National Natural Science Foundation of China(21576050)the Natural Science Foundation of Jiangsu Province(BK20150604)~~
文摘Au-Ag bimetallic nanoparticle‐supported microporous titanium silicalite‐1catalysts were prepared via a hydrothermal‐immersion method,and their structures were examined.These materials serve as efficient catalysts for the photosynthesis of propylene oxide via the epoxidation of propene.The Au/Ag mass ratio and reaction temperature were demonstrated to have significant effects on the catalytic activity and selectivity of propylene oxide.The optimal formation rate(68.3μmol/g·h)and selectivity(52.3%)toward propylene oxide were achieved with an Au:Ag mass ratio of4:1.Notably,the strong synergistic effect between Au and Ag resulted in superior photocatalysis of the bimetallic systems compared with those of the individual systems.A probable reaction mechanism was proposed based on the theoretical and experimental results.
文摘Selective and durable fixed‐bed catalysts are highly desirable for developing eco‐efficient HPPO(hydrogen peroxide propylene oxide)process.The powder titanosilicate catalysts must be shaped before being applied in industrial processes.As the essential additives for preparing formed catalysts,binders are usually the catalytically inert components,but they would cover the surface and pore mouth of zeolite,thereby declining the accessibility of active sites.By recrystallizing the binder(silica)/Ti‐MWW extrudates with the assistance of dual organic structure‐directing agents,the silica binder was converted into MWW zeolite phase to form a structured binder‐free Ti‐MWW zeolite with Si‐rich shell,which enhanced the diffusion efficiency and maintained the mechanical strength.Meanwhile,due to the partial dissolution of Si in the Ti‐MWW matrix,abundant silanol nests formed and part of framework TiO4 species were transferred into open TiO_(6)ones,improving the accumulation and activation ability of H_(2)O_(2)inside the monolith.Successive piperidine treatment and fluoridation of the binder‐free Ti‐MWW further enhanced the H_(2)O_(2)activation and oxygen transfer ability of the active Ti sites,and stabilized the Ti‐OOH intermediate through hydrogen bond formed between the end H in Ti‐OOH and the adjacent Si‐F species,thus achieving a more efficient epoxidation process.Additionally,the side reaction of PO hydrolysis was inhibited because the modification effectively quenched numerous Si‐OH groups.The lifetime of the modified binder‐free Ti‐MWW catalyst was 2400 h with the H_(2)O_(2)conversion and PO selectivity both above 99.5%.
基金the financial support of the State Basic Research Project ‘‘973’’ by the Ministry of Science and Technology of People’s Republic of China (2006CB202508)
文摘Hollow titanium silicalite （HTS） molecular sieve has been synthesized, and information on its structure, physico- chemical characterization, as well as surface property was investigated by a host of analytical methods, such as XRF, XRD, low-temperature N2 adsorption/desorption, TEM, FT-IR, UV-Vis, 29Si MAS NIVIR, and XPS techniques. The characterization results suggest that HTS zeolite has a special hollow crystal structure and its mesopore volume is larger than that of TS-1 zeolite. The titanium species in this zeolite are composed of the framework tetrahedral Ti （IV） ions and extra-framework octahedral Ti （IV） ions, which tend to disperse into its bulk phase. This zeolite material also has been applied to catalyze the cyclohexanone oxidation process, and the products are not completely consistent with those results obtained by using TS-1 zeolite, which might be caused by their difference in pore structure and pore volume, especially the mesopore volume. Cy- clohexanone oxidation catalyzed by HTS zeolite is a representative consecutive reaction, the main target products of which are e-caprolactone, 6-hydroxyhexanoic acid and adipic acid. The effect of H202/cyclohexanone mole ratio on the cyclohexa- none conversion, the total target product selectivity, the distribution of three target products selectivity and their variations along with reaction time is also researched and analyzed, which indicate that HTS zeolite shows a high performance for the Baeyer-Villiger reaction of cyclohexanone and catalytic oxidation of 6-hydroxyhexanoic acid under mild conditions, and the quantity of active surface titanium species as well as the pore structure and mesopore volume controlling the mass diffusion rate are the key factors determining the catalytic activity of HTS zeolite and product selectivity.
基金Project supported by the National Science Foundation of China(2006CB202508)
文摘29Si-NMR and 1H-NMR were used to follow up the basic hydrolysis of tetraethyl orthosilicate （TOES） and the results showed that species of monomer, dimer, trimer, cyclic and polymer silicates were formed. The monomer and dimer were favorable for the high activity of zeolite. XRD, 13C CP/MAS and 29Si NMR were used to trace the crystallization process of hollow titanium silicalite zeolites （HTS）. The results showed that the induction period of HTS was 80 min, and subsequently it took next 10 min to form HTS and the remaining time of the crystallization period might function for cleaning up the pores and/or washing off the impurities from the HTS zeolite. The catalytic oxidation performance of HTS zeolite is different from that of the acid activity of zeolite in which the conventional definition of crystallinity does not reflect the catalytic oxidation activity proportionally. The synthesized HTS samples were character- ized by XRD, FT-IR, UV-Vis and Raman spectra. It was confirmed that Ti was incorporated into the zeolite framework. The synthesized HTS samples revealed good repeatability and high activity for oxidation of phenol into diphenol.
