The surfaces of galena and pyrite,the adsorption of oxygen,and the reactions of ethyl xanthate on the sulfides were studied using quantum chemical calculations.In addition,the surface electron structures of the minera...The surfaces of galena and pyrite,the adsorption of oxygen,and the reactions of ethyl xanthate on the sulfides were studied using quantum chemical calculations.In addition,the surface electron structures of the minerals were discussed.According to the results,the mechanisms of ionic exchange reaction and dixanthogen adsorption for the xanthate notation of galena and pyrite were explained.The important role of oxygen in collector and collectorless flotation processes was also investigated.展开更多
Three different zeolite catalysts with different pore sizes(MFI-type,BEA-type,and FAU-type zeolites)have been prepared.The influence of different zeolite catalysts on reactivity and product shape selectivity of tetral...Three different zeolite catalysts with different pore sizes(MFI-type,BEA-type,and FAU-type zeolites)have been prepared.The influence of different zeolite catalysts on reactivity and product shape selectivity of tetralin is investigated.Clear differences are observed in the reactivity of tetralin and distribution of products achieved by different catalysts.The diffusion and adsorption behavior of the reactant tetralin and its intermediates,n-butylbenzene and 1-methylindane under the reaction conditions are simulated using molecular simulation methods.Upon combining simulation results and experimental observations,it is shown that the difference in diffusion coefficient and competitive adsorption capacity can explain the reactivity of tetralin and the selectivity of products.The steric hindrance of the MFI-type zeolite mainly limits the key step of ring opening of tetralin,leading to lower selectivity of ring-opening products.n-Butylbenzene molecules can diffuse sufficiently fast in the large pores of FAU-type zeolite and the weak adsorption capacity of n-butylbenzene leads to its insufficient cracking.In addition,it also explains the reason that the BEA-type zeolite has the best BTX selectivity,because it can satisfy both good ring-opening activity and sufficient butylbenzene cracking depth.展开更多
We have measured directly the low field magnetization and its time decay of weak link superconductor in the sintered T1_(2)Ba_(2)Ca_(2)Cu_(3)O_(10+x).The decay of magnetization with time at the field intensities of 5,...We have measured directly the low field magnetization and its time decay of weak link superconductor in the sintered T1_(2)Ba_(2)Ca_(2)Cu_(3)O_(10+x).The decay of magnetization with time at the field intensities of 5,10,15,20 and 50 Oe was observed to follow the law of logarithm,M∝Int.The pinning potential derived from the slope of the magnetization decay is about 0.045~0.075eV.展开更多
The support γ-Al_2O_3 was treated with 1-methylnaphthalene as the model reactant by respectively using the chemical static adsorption method and the accelerated coking method to study the coking sites of γ-Al_2O_3 s...The support γ-Al_2O_3 was treated with 1-methylnaphthalene as the model reactant by respectively using the chemical static adsorption method and the accelerated coking method to study the coking sites of γ-Al_2O_3 surface. The carbon species formed on γ-Al_2O_3 surface were analyzed by CAT-CS, TG-MS, IR-OH, and Py-IR techniques. The results of characterization by CAT-CS and TG-MS techniques indicated that the carbon species formed during the chemical static adsorption process is mainly composed of the reversibly adsorbed coke precursors with a lowly-condensed state, while that formed after the accelerated coking process is probably related with the irreversibly adsorbed coke deposits with a highlycondensed state. The results of characterization by IR-OH and Py-IR techniques further implied that the formation of the two kinds of carbon species, i.e., coke precursors and coke deposits, are closely related with the basic hydroxyl groups and the strong Lewis acid sites on γ-Al_2O_3 surface. The results lead to a deep insight into the coking mechanism on the alumina surface.展开更多
文摘The surfaces of galena and pyrite,the adsorption of oxygen,and the reactions of ethyl xanthate on the sulfides were studied using quantum chemical calculations.In addition,the surface electron structures of the minerals were discussed.According to the results,the mechanisms of ionic exchange reaction and dixanthogen adsorption for the xanthate notation of galena and pyrite were explained.The important role of oxygen in collector and collectorless flotation processes was also investigated.
文摘Three different zeolite catalysts with different pore sizes(MFI-type,BEA-type,and FAU-type zeolites)have been prepared.The influence of different zeolite catalysts on reactivity and product shape selectivity of tetralin is investigated.Clear differences are observed in the reactivity of tetralin and distribution of products achieved by different catalysts.The diffusion and adsorption behavior of the reactant tetralin and its intermediates,n-butylbenzene and 1-methylindane under the reaction conditions are simulated using molecular simulation methods.Upon combining simulation results and experimental observations,it is shown that the difference in diffusion coefficient and competitive adsorption capacity can explain the reactivity of tetralin and the selectivity of products.The steric hindrance of the MFI-type zeolite mainly limits the key step of ring opening of tetralin,leading to lower selectivity of ring-opening products.n-Butylbenzene molecules can diffuse sufficiently fast in the large pores of FAU-type zeolite and the weak adsorption capacity of n-butylbenzene leads to its insufficient cracking.In addition,it also explains the reason that the BEA-type zeolite has the best BTX selectivity,because it can satisfy both good ring-opening activity and sufficient butylbenzene cracking depth.
文摘We have measured directly the low field magnetization and its time decay of weak link superconductor in the sintered T1_(2)Ba_(2)Ca_(2)Cu_(3)O_(10+x).The decay of magnetization with time at the field intensities of 5,10,15,20 and 50 Oe was observed to follow the law of logarithm,M∝Int.The pinning potential derived from the slope of the magnetization decay is about 0.045~0.075eV.
基金support from the National Key Basic Research Program of China (Grant 2017YFB0306603)
文摘The support γ-Al_2O_3 was treated with 1-methylnaphthalene as the model reactant by respectively using the chemical static adsorption method and the accelerated coking method to study the coking sites of γ-Al_2O_3 surface. The carbon species formed on γ-Al_2O_3 surface were analyzed by CAT-CS, TG-MS, IR-OH, and Py-IR techniques. The results of characterization by CAT-CS and TG-MS techniques indicated that the carbon species formed during the chemical static adsorption process is mainly composed of the reversibly adsorbed coke precursors with a lowly-condensed state, while that formed after the accelerated coking process is probably related with the irreversibly adsorbed coke deposits with a highlycondensed state. The results of characterization by IR-OH and Py-IR techniques further implied that the formation of the two kinds of carbon species, i.e., coke precursors and coke deposits, are closely related with the basic hydroxyl groups and the strong Lewis acid sites on γ-Al_2O_3 surface. The results lead to a deep insight into the coking mechanism on the alumina surface.
