Hydrogen transfer is an important secondary reaction of catalytic cracking reactions, which affects product yield distribution and product quality. It is an exothermic reaction with low activation energy around 43.3 k...Hydrogen transfer is an important secondary reaction of catalytic cracking reactions, which affects product yield distribution and product quality. It is an exothermic reaction with low activation energy around 43.3 kJ/mol. Catalyst properties and operation parameters in catalytic cracking greatly influence the hydrogen transfer reaction. Satisfactory results are expected through careful selection of proper catalysts and operation conditions.Fluid catalytic cracking (FCC) is one of the major refining processes for converting vacuum distillates and residues into gas, high octane gasoline and diesel fuels over solid acidic catalysts. Cracking catalyst promotes cracking reactions, the reaction mechanism can be explained by carbonium ion theory [1] . Hydrogen transfer is a bimolecular reaction which requires two adjacent acid sites, where hydrogen usually transfers from a heavier hydrocarbon molecule to a lighter alkene molecule, the latter desorbs as an isoalkane molecule, and the former that donates hydrogen becomes more aromatic and finally coke [2] . Hydrogen transfer activity has long been recognized as relating to the acid site density of the catalyst. Thus the alkene content and composition of cracked naphtha and of product gas are expected to be adjusted by hydrogen transfer reaction occurred in FCC process. In this study, many factors affecting hydrogen transfer reaction, such as different kinds of zeolite catalysts used, reaction temperature, reaction time and coke deposit, were investigated. It will be helpful for the refiners to control proper extent of hydrogen transfer reaction in FCC process operation to adapt to different purposes and various options, such as maximizing gasoline yield, maximizing or minimizing olefins in gasoline, maximizing or minimizing gas olefins or iso olefins in product etc..展开更多
甲烷作为全球第二大温室气体,是典型的可再生清洁能源,也是碳循环中的重要物质组成。大气中约74%的甲烷由产甲烷古菌和其他微生物的互营产生,种间电子传递(interspecies electron transfer, IET)是微生物菌群降低热力学能垒、实现互营...甲烷作为全球第二大温室气体,是典型的可再生清洁能源,也是碳循环中的重要物质组成。大气中约74%的甲烷由产甲烷古菌和其他微生物的互营产生,种间电子传递(interspecies electron transfer, IET)是微生物菌群降低热力学能垒、实现互营产甲烷的核心过程。IET可分为间接种间电子传递(mediated interspecies electron transfer,MIET)和直接种间电子传递(direct interspecies electron transfer, DIET)两种类型,其中MIET依赖氢气、甲酸等载体完成电子的远距离传输,而DIET则依赖导电菌毛、细胞色素c等膜蛋白,通过微生物的直接接触实现电子传递。本文将从IET的研究历程出发,从电子传递机制、微生物种类、生态多样性等方面对微生物互营产甲烷过程中的两种IET类型进行比较,最后对未来待探索的方向进行展望。本综述有助于加深对微生物互营产甲烷过程中IET的理解,为解决由甲烷引发的全球气候变暖等生态问题提供理论支撑。展开更多
Numerical studies under supercritical pressure are carried out to study the heat transfer characteristics in a single-root coolant channel of the active regenerative cooling system of the scramjet engine, using actual...Numerical studies under supercritical pressure are carried out to study the heat transfer characteristics in a single-root coolant channel of the active regenerative cooling system of the scramjet engine, using actual physical properties of pentane. The relationships between wall temperature and inlet temperature, mass flow rate, wall heat flux, inlet pressure, as well as center stream temperature are obtained. The results suggest that the heat transfer deterioration occurs when the fuel temperature approaches the pseudo-critical temperature, and the wall temperature increases rapidly and heat transfer coefficient decreases sharply. The decrease of wall heat flux, as well as the increase of mass flow rate and inlet pressure makes the starting point of the heat transfer deterioration and the peak point of the wall temperature move backward. The wall temperature increment induced by heat transfer deterioration decreases, which could reduce the severity of the heat transfer deterioration. The relational expression of the heat transfer deterioration critical heat flux derives from the relationship of the mass flow rate and the inlet pressure.展开更多
In this work a novel strategy has been developed to prepare well-dispersed amine-functionalized SiO2 nanodot-coated layered double hydroxide nano- composite （NH2-SiO2@LDH） via electrostatic interactions and condensa...In this work a novel strategy has been developed to prepare well-dispersed amine-functionalized SiO2 nanodot-coated layered double hydroxide nano- composite （NH2-SiO2@LDH） via electrostatic interactions and condensation of （3-aminopropyl）triethoxysilane （APTES）. This nanocomposite system is well dispersed in culture media and phosphate buffered saline, and exhibits low cytotoxicity and good biocompatibility. The fluorescence microscopy images and flow cytometry data indicate that such an NH2-SiO2@LDH nanocomposite is able to efficiently deliver small interfering RNA （siRNA） into the U2OS cell line to inhibit cell proliferation. Thus, NH2-SiOR@LDH nanocomposite has a great potential as a nanocarrier for efficient gene delivery.展开更多
Developing efficient,stable,and low-cost novel electron-cocatalysts is crucial for photocatalytic hydrogen evolution reaction.Herein,amorphous Ni-P alloy particles were successfully modified onto g-C3N4 to construct t...Developing efficient,stable,and low-cost novel electron-cocatalysts is crucial for photocatalytic hydrogen evolution reaction.Herein,amorphous Ni-P alloy particles were successfully modified onto g-C3N4 to construct the Ni-P/g-C3N4 photocatalyst through a simple and green triethanolamine(TEOA)-mediated photodeposition method.It was found that the TEOA could serve as an excellent complexing agent to coordinate with Ni2+to form[Ni(TEOA)]^2+complex,which can promote the rapid and effective deposition of amorphous Ni-P alloy on the g-C3N4 surface.Photocatalytic tests suggest that the hydrogen-evolution performance of gC3N4 can be greatly promoted through integrating amorphous Ni-P alloy.Especially,the Ni-P/g-C3N4(5 wt%)exhibits the superior H2-generation activity(118.2μmol h^-1g^-1),which is almost 35.8 times that of bare g-C3N4.Furthermore,the amorphous Ni-P alloy cocatalyst can also serve as the general hydrogen-production cocatalyst to greatly enhance the photocatalytic performance of traditional semiconductor materials such as Ti O2 and Cd S.Based on the present results,the mechanism of the amorphous Ni-P alloy as the high-efficiency electron transfer medium was proposed for the boosted H2-generation rate.The present facile route may broaden the horizons for the efficient development of highly active cocatalysts in photocatalytic field.展开更多
文摘Hydrogen transfer is an important secondary reaction of catalytic cracking reactions, which affects product yield distribution and product quality. It is an exothermic reaction with low activation energy around 43.3 kJ/mol. Catalyst properties and operation parameters in catalytic cracking greatly influence the hydrogen transfer reaction. Satisfactory results are expected through careful selection of proper catalysts and operation conditions.Fluid catalytic cracking (FCC) is one of the major refining processes for converting vacuum distillates and residues into gas, high octane gasoline and diesel fuels over solid acidic catalysts. Cracking catalyst promotes cracking reactions, the reaction mechanism can be explained by carbonium ion theory [1] . Hydrogen transfer is a bimolecular reaction which requires two adjacent acid sites, where hydrogen usually transfers from a heavier hydrocarbon molecule to a lighter alkene molecule, the latter desorbs as an isoalkane molecule, and the former that donates hydrogen becomes more aromatic and finally coke [2] . Hydrogen transfer activity has long been recognized as relating to the acid site density of the catalyst. Thus the alkene content and composition of cracked naphtha and of product gas are expected to be adjusted by hydrogen transfer reaction occurred in FCC process. In this study, many factors affecting hydrogen transfer reaction, such as different kinds of zeolite catalysts used, reaction temperature, reaction time and coke deposit, were investigated. It will be helpful for the refiners to control proper extent of hydrogen transfer reaction in FCC process operation to adapt to different purposes and various options, such as maximizing gasoline yield, maximizing or minimizing olefins in gasoline, maximizing or minimizing gas olefins or iso olefins in product etc..
文摘甲烷作为全球第二大温室气体,是典型的可再生清洁能源,也是碳循环中的重要物质组成。大气中约74%的甲烷由产甲烷古菌和其他微生物的互营产生,种间电子传递(interspecies electron transfer, IET)是微生物菌群降低热力学能垒、实现互营产甲烷的核心过程。IET可分为间接种间电子传递(mediated interspecies electron transfer,MIET)和直接种间电子传递(direct interspecies electron transfer, DIET)两种类型,其中MIET依赖氢气、甲酸等载体完成电子的远距离传输,而DIET则依赖导电菌毛、细胞色素c等膜蛋白,通过微生物的直接接触实现电子传递。本文将从IET的研究历程出发,从电子传递机制、微生物种类、生态多样性等方面对微生物互营产甲烷过程中的两种IET类型进行比较,最后对未来待探索的方向进行展望。本综述有助于加深对微生物互营产甲烷过程中IET的理解,为解决由甲烷引发的全球气候变暖等生态问题提供理论支撑。
基金the funding supports from National Natural Science Foundation of China (Grant No.51076035 and No.11079017), HIT.NSRIF.2008. 24
文摘Numerical studies under supercritical pressure are carried out to study the heat transfer characteristics in a single-root coolant channel of the active regenerative cooling system of the scramjet engine, using actual physical properties of pentane. The relationships between wall temperature and inlet temperature, mass flow rate, wall heat flux, inlet pressure, as well as center stream temperature are obtained. The results suggest that the heat transfer deterioration occurs when the fuel temperature approaches the pseudo-critical temperature, and the wall temperature increases rapidly and heat transfer coefficient decreases sharply. The decrease of wall heat flux, as well as the increase of mass flow rate and inlet pressure makes the starting point of the heat transfer deterioration and the peak point of the wall temperature move backward. The wall temperature increment induced by heat transfer deterioration decreases, which could reduce the severity of the heat transfer deterioration. The relational expression of the heat transfer deterioration critical heat flux derives from the relationship of the mass flow rate and the inlet pressure.
文摘In this work a novel strategy has been developed to prepare well-dispersed amine-functionalized SiO2 nanodot-coated layered double hydroxide nano- composite （NH2-SiO2@LDH） via electrostatic interactions and condensation of （3-aminopropyl）triethoxysilane （APTES）. This nanocomposite system is well dispersed in culture media and phosphate buffered saline, and exhibits low cytotoxicity and good biocompatibility. The fluorescence microscopy images and flow cytometry data indicate that such an NH2-SiO2@LDH nanocomposite is able to efficiently deliver small interfering RNA （siRNA） into the U2OS cell line to inhibit cell proliferation. Thus, NH2-SiOR@LDH nanocomposite has a great potential as a nanocarrier for efficient gene delivery.
基金supported by the National Natural Science Foundation of China(21771142 and 51672203)the Fun-damental Research Funds for the Central Universities(WUT 2019IB002)。
文摘Developing efficient,stable,and low-cost novel electron-cocatalysts is crucial for photocatalytic hydrogen evolution reaction.Herein,amorphous Ni-P alloy particles were successfully modified onto g-C3N4 to construct the Ni-P/g-C3N4 photocatalyst through a simple and green triethanolamine(TEOA)-mediated photodeposition method.It was found that the TEOA could serve as an excellent complexing agent to coordinate with Ni2+to form[Ni(TEOA)]^2+complex,which can promote the rapid and effective deposition of amorphous Ni-P alloy on the g-C3N4 surface.Photocatalytic tests suggest that the hydrogen-evolution performance of gC3N4 can be greatly promoted through integrating amorphous Ni-P alloy.Especially,the Ni-P/g-C3N4(5 wt%)exhibits the superior H2-generation activity(118.2μmol h^-1g^-1),which is almost 35.8 times that of bare g-C3N4.Furthermore,the amorphous Ni-P alloy cocatalyst can also serve as the general hydrogen-production cocatalyst to greatly enhance the photocatalytic performance of traditional semiconductor materials such as Ti O2 and Cd S.Based on the present results,the mechanism of the amorphous Ni-P alloy as the high-efficiency electron transfer medium was proposed for the boosted H2-generation rate.The present facile route may broaden the horizons for the efficient development of highly active cocatalysts in photocatalytic field.
