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Optimization of Mg-based hydrogen storage materials with multicomponent and high-entropy catalysts 被引量:1
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作者 Yu Sun Jiayi Cheng +2 位作者 Yaru Jiang Yafei Liu Yijing Wang 《International Journal of Minerals,Metallurgy and Materials》 2025年第11期2699-2712,共14页
Novel hydrogen storage materials have propelled progress in hydrogen storage technologies.Magnesium hydride(MgH_(2))is a highly promising candidate.Nevertheless,several drawbacks,including the need for elevated therma... Novel hydrogen storage materials have propelled progress in hydrogen storage technologies.Magnesium hydride(MgH_(2))is a highly promising candidate.Nevertheless,several drawbacks,including the need for elevated thermal conditions,sluggish dehydrogena-tion kinetics,and high thermodynamic stability,limit its practical application.One effective method of addressing these challenges is cata-lyst doping,which effectively boosts the hydrogen storage capability of Mg-based materials.Herein,we review recent advancements in catalyst-doped MgH_(2) composites,with particular focus on multicomponent and high-entropy catalysts.Structure-property relationships and catalytic mechanisms in these doping strategies are also summarized.Finally,based on existing challenges,we discuss future research directions for the development of Mg-based hydrogen storage systems. 展开更多
关键词 magnesium hydride multicomponent materials high-entropy materials hydrogen storage catalyst doping kinetics
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Synthesis and Properties of Photodegradable Poly(furan-amine)s by a Catalyst-free Multicomponent Cyclopolymerization 被引量:1
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作者 Wei-Qiang Fu Gui-Nan Zhu +3 位作者 Jian-Bing Shi Bin Tong Zheng-Xu Cai Yu-Ping Dong 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2019年第10期981-989,I0004,共10页
A series of new photodegradable poly(furan-amine)s(PFAs) were synthesized by a one-pot, catalyst-free, multicomponent cyclopolymerization between diisocyanides, dialkylacetylene dicarboxylates, and aromatic dialdehyde... A series of new photodegradable poly(furan-amine)s(PFAs) were synthesized by a one-pot, catalyst-free, multicomponent cyclopolymerization between diisocyanides, dialkylacetylene dicarboxylates, and aromatic dialdehydes. All polymerizations were conducted in toluene at 100 ℃ for 6 h without inert gas protection and furnished polymers with a satisfactory molecular weight(Mw up to32200) and yield. The PFA structure was confirmed by spectroscopic techniques, such as GPC, FTIR, and NMR, as well as by comparison with a model compound. The polymers exhibited good solubility in common organic solvents and thermal stability. All the PFAs had high refractive indices in the visible light region(400 nm to 800 nm). Moreover, the PFAs were substantially degraded by UV irradiation due to the presence of furan rings. The film thickness reduction rate could be over 90%. 展开更多
关键词 PHOTODEGRADATION multicomponent reaction catalyst-FREE POLYMERIZATION
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Deactivation of Ti-La-Li Multicomponent OxideCatalyst for Oxidative Coupling of Methane
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作者 ZHAO Zhen and YUAN Song-yue(Changchun Institute of Applied Chemistry, Academia Sinica, Changchun. 130022)YU Zuo-long(Chengdu Institute of Organic Chemistry , Academia Sinica, Chengdu, 610015) 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 1994年第4期321-326,共6页
he deactivation of highly active multicomponent oxide LiLa_0.5 Ti_0.5 O_(2+λ) cata-lyst at high reaction temperatures has been studied. The surface and bulk structureof the catalyst were characterized by means of XRD... he deactivation of highly active multicomponent oxide LiLa_0.5 Ti_0.5 O_(2+λ) cata-lyst at high reaction temperatures has been studied. The surface and bulk structureof the catalyst were characterized by means of XRD, IR, XPS, BET, O_2-TPD,SEM etc.. The results show that the deactivation of the catalyst at high reactiontemperatures is mainly due to the loss of surface lithium. As a result , the diffusionof lithium from bulk to surface leads to the decompositiqn of the active phase con-taining lithium, which lowers tlie number of oxygen vacancies and decreases themobility of lattice oxygen. 展开更多
关键词 catalyst Oxidative coupling of methane DEACTIVATION Titanium-Lan-thanum-Lithium multicomponent oxide
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Silica supported perchloric acid(HClO_4-SiO_2):A mild,reusable and highly efficient heterogeneous catalyst for the synthesis of amidoalkyl naphthols 被引量:7
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作者 Gholam Hossein Mahdavinia Mohammad A.Bigdeli Majid M.Heravi 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第10期1171-1174,共4页
An efficient and direct procedure has been developed for the preparation of amidoalkyl naphthols by a one-pot condensation of aryl aldehydes, 2-naphthol and urea or amides, in the presence of HClO4-SiO2 as a heterogen... An efficient and direct procedure has been developed for the preparation of amidoalkyl naphthols by a one-pot condensation of aryl aldehydes, 2-naphthol and urea or amides, in the presence of HClO4-SiO2 as a heterogeneous catalyst. The reactions were carried out under reflux and solvent-free conditions. The present methodology offers several advantages such as excellent yields, simple procedure, easy work-up and ecofriendly reaction condition. The catalyst is easily prepared, stable, reusable and efficient under the reaction conditions. 展开更多
关键词 ONE-POT HClO4-SiO2 Heterogeneous catalyst Amidoalkyl naphthol multicomponent reaction
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A green multicomponent synthesis of bioactive pyrimido[4,5-b]quinoline derivatives as antibacterial agents in water catalyzed by RuCl_3·xH_2O 被引量:3
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作者 Khalil Tabatabaeian Abdollah Fallah Shojaei +2 位作者 Farhad Shirini Seyyedeh Zoha Hejazi Mehdi Rassa 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第2期308-312,共5页
An efficient, convenient and environmentally benign one-pot multicomponent reaction for the preparation of pyrimido[4,5-b]quinoline derivatives as biologically, pharmacologically and antibacte- rially active products ... An efficient, convenient and environmentally benign one-pot multicomponent reaction for the preparation of pyrimido[4,5-b]quinoline derivatives as biologically, pharmacologically and antibacte- rially active products has been developed using RuC13.xH20 as a reusable homogenous catalyst. Use of water as a green solvent, purification of products by non-chromatographic methods, reusability of transition metal homogenous catalyst, saving energy by employing multicomponent reactions, short reaction times and high yields, are some of the advantages of this process. 展开更多
关键词 Pyrimido[4 5-b]quinoline Reusable homogenous catalyst One-pot multicomponent reaction Antibacterial activity WATER
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Catalytic conversion and DFT analysis of post DDBD-catalysis system for degradation of toluene,ethyl acetate and acetone with different metal-oxides catalysts 被引量:2
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作者 Xin Liu Jianqi Liu +1 位作者 Jiayao Chen Fangchuan Zhong 《Journal of Rare Earths》 SCIE EI CAS CSCD 2023年第2期215-223,共9页
A series of multiphase metal-oxide catalysts(MnOx/γ-Al_(2)O_(3),CuOx/γ-Al_(2)O_(3),FeO_(x/γ)-Al_(2)O_(3),CeO_(x)/γ-Al_(2)O_(3)and LaOx/γ-Al_(2)O_(3))were prepared for plasma-catalyst degradation of multicomponent... A series of multiphase metal-oxide catalysts(MnOx/γ-Al_(2)O_(3),CuOx/γ-Al_(2)O_(3),FeO_(x/γ)-Al_(2)O_(3),CeO_(x)/γ-Al_(2)O_(3)and LaOx/γ-Al_(2)O_(3))were prepared for plasma-catalyst degradation of multicomponent volatile organic compounds(VOCs,such as toluene,acetone and ethyl acetate).The results reveal that the degradation efficiency(DE)of acetone,toluene and ethyl acetate in the DDBD system can be arranged as follows:Mn_(2)O_(3)/γ-Al_(2)O_(3)>Fe2O3/γ-Al_(2)O_(3)>CuO_(/γ)-Al_(2)O_(3)>CeO_(2)/γ-Al_(2)O_(3)>La_(2)O_(3)/γ-Al_(2)O_(3)>γ-Al_(2)O_(3),and the highest DE(49.5%for acetone,93.3%for toluene and 79.8%for ethyl acetate)is obtained in Mn_(2)O_(3)/γ-Al_(2)O_(3)+double dielectric barrier discharge(DDBD)system at specific input energy(SIE)of 700 J/L.Compared with the other catalysts,Mn_(2)O_(3)/γ-Al_(2)O_(3)also exhibits the most significant inhibitory effect on the production of ozone(O3).On the other hand,CeO_(2)/γ-Al_(2)O_(3)and La_(2)O_(3)/γ-Al_(2)O_(3)catalysts display different catalytic selectivity.Both catalysts can slightly raise the DE of VOCs and remarkably facilitate VOCs’mineralization.The carbon balance(CB)is increased by 30.2%and 38.8%,and the CO_(2)selectivity(SCO_(2))is raised by 70.5%and 11.9%in the CeO_(2)/γ-Al_(2)O_(3)+DDBD system and La_(2)O_(3)/γ-Al_(2)O_(3)+DDBD system at SIE of 700 J/L,respectively.To further understand the catalytic effect of the catalysts,the adsorption of O3on different catalysts was simulated by a DFT model.According to the results of the DFT model,it is found that the adsorption energy of other metal oxides seems to be used as a reference for catalytic effect to a certain extent except CeO_(2).The higher the absolute values of adsorption energy,the higher the improvement of VOCs degradation efficiency by catalyst. 展开更多
关键词 Multiphase metal-oxide catalysts Plasma-catalyst multicomponent volatile organic compounds Rare earths
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SnCl_2/nano SiO_2: A green and reusable heterogeneous catalyst for the synthesis of polyfunctionalized 4H-pyrans 被引量:2
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作者 Javad Safaei-Ghomi Raheleh Teymuri +1 位作者 Hossein Shahbazi-Alavi Abolfazl Ziarati 《Chinese Chemical Letters》 SCIE CAS CSCD 2013年第10期921-925,共5页
A highly efficient and general method for the synthesis of polyfunctionalized 4H-pyrans is established through a one-pot multicomponent cyclocondensation of aromatic aldehydes with CH acids, malononitrile and ethyl ac... A highly efficient and general method for the synthesis of polyfunctionalized 4H-pyrans is established through a one-pot multicomponent cyclocondensation of aromatic aldehydes with CH acids, malononitrile and ethyl acetoacetate using nano silica supported tin (II) chloride as a catalyst. In this method SnCl2/nano Si02 was used as green and reusable catalyst. Excellent yields, short reaction times, simple workup, and inexpensiveness and commercially availability of the catalyst are the advantages of this method. 展开更多
关键词 Nano silica supported tin (11) chloride Polyfunctionalized 4H-pyrans multicomponent reactions Heterogeneous catalyst
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Efficient synthesis of pyrano[2,3-d]pyrimidinone and pyrido[2,3-d]pyrimidine derivatives in presence of novel basic ionic liquid catalyst 被引量:1
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作者 Omid Goli Jolodar Farhad Shirini Mohadeseh Seddighi 《Chinese Journal of Catalysis》 CSCD 北大核心 2017年第7期1245-1251,共7页
A basic ionic liquid, namely 1,1'-(butane-1,4-diyl)bis(1,4-diazabicyclo [2.2.2]octan-1-ium) hydrox-ide, was prepared and characterized using Fourier-transform infrared spectroscopy, XH nuclear magnetic... A basic ionic liquid, namely 1,1'-(butane-1,4-diyl)bis(1,4-diazabicyclo [2.2.2]octan-1-ium) hydrox-ide, was prepared and characterized using Fourier-transform infrared spectroscopy, XH nuclear magnetic resonance spectroscopy, and pH measurements. The ionic liquid was used for efficient promotion of the synthesis of pyrano[2,3-d]pyrimidinone and pyrido[2,3-d]pyrimidine derivatives at room temperature under grinding conditions. A simple procedure, short reaction time, high yields, non-column chromatographic separation, commercial availability of the starting materials, and recyclability of the catalyst are attractive features of this process. 展开更多
关键词 Basic catalyst multicomponent reaction Pyrimidine derivative GRINDING
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First example of multicomponent synthesis of 1-ethoxy-3-(4-aryl)-1-phenyl- 1H-benzo[f]-chromene derivatives
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作者 Saman Damavandi Reza Sandaroos +1 位作者 Majid Vafaeei Hamid Reza Molaei 《Chinese Chemical Letters》 SCIE CAS CSCD 2012年第3期253-256,共4页
A new series of 1-ethoxy-3-(4-aryl)-1-phenyl-1H-benzo[f]chromenes have been synthesized efficiently.The procedure involves the multicomponent reaction of 2-naphthol,acetophenone derivatives,and triethyl orthobenzoat... A new series of 1-ethoxy-3-(4-aryl)-1-phenyl-1H-benzo[f]chromenes have been synthesized efficiently.The procedure involves the multicomponent reaction of 2-naphthol,acetophenone derivatives,and triethyl orthobenzoate catalyzing by efficient bis(2-anilinotropone) Ti complex. 展开更多
关键词 multicomponent reaction Benzo[f]chromen catalyst
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Disclosing the active integration structure and robustness of a pseudo-tri-component electrocatalyst toward alkaline hydrogen evolution
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作者 Hong-Hong Zou Wan-Qing Li +7 位作者 Cong-Hu Song Li-Ming Cao Xue-Feng Zhang Xuan-Yi Zhu Zi-Yi Du Jia Zhang Sheng-Liang Zhong Chun-Ting He 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2022年第9期210-216,I0007,共8页
Designing multicomponent integration catalysts(MICs)has been a promising strategy for improving electrocatalytic hydrogen evolution reaction(HER)due to the highly active interfaces as well as electronic synergy.Nevert... Designing multicomponent integration catalysts(MICs)has been a promising strategy for improving electrocatalytic hydrogen evolution reaction(HER)due to the highly active interfaces as well as electronic synergy.Nevertheless,many fundamental questions such as their actual active species and the influence on long-term stability remain to be answered.Herein,we present the structural evolution from a pseudotri-component electrocatalyst of nitrogen-doped carbon supported nickel/vanadium nitride/vanadium oxide(Ni-VN-V_(2)O_(3)/NC)nanorods to the heterostructural nickel/vanadium nitride(Ni-VN/NC)nanosheets during chemical or electrochemical processes.The self-reconstructed Ni-VN/NC exhibits a robust stability under alkaline conditions,while maintaining initial efficient HER activity with a low overpotential of 76 mV at the current density of 10 mA cm^(-2).Theoretical calculations and quasi-in-situ spectroscopic technology unveil the redistribution of electrons on the synergistic active interface,which synchronously optimizes the affinities for hydrogen,hydroxide,and water molecules,thereby remarkably accelerating the HER kinetics by reducing the barrier of Volmer step. 展开更多
关键词 Hydrogen evolution reaction multicomponent integration catalysts Structural transformation ELECTROCATALYSIS Density functional theory
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Distereoselective one-pot synthesis of pyrimidopyrimidines using sulfated tin oxide as a reusable catalyst:An extension of Biginelli-type reaction
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作者 Rupali L.Magar Prashant B.Thorat +3 位作者 Pratima B.Thorat Vinod V.Thorat Bhagawan R.Patil Rajendra P.Pawar 《Chinese Chemical Letters》 SCIE CAS CSCD 2013年第12期1070-1074,共5页
The Biginelli-type compounds 4,5,8a-triarylhexahydropyrimido[4,5-d]pyrimidine-2,7(1H,3H)-diones were synthesized by a one-pot three-component reaction using sulfated tin oxide as a reusable catalyst. This method has... The Biginelli-type compounds 4,5,8a-triarylhexahydropyrimido[4,5-d]pyrimidine-2,7(1H,3H)-diones were synthesized by a one-pot three-component reaction using sulfated tin oxide as a reusable catalyst. This method has the advantages of high yields, short reaction time, simple starting materials and reusability of catalyst for several times. 展开更多
关键词 Biginelli-type reaction multicomponent reactions Pyrimido[4 5-d]pyrimidine Sulfated tin oxide Reusable catalyst
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Sulfuric Acid Immobilized on Silica Gel as Highly Efficient and Heterogeneous Catalyst for the One-Pot Synthesis of 2,4,5-Triaryl-1H-imidazoles
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作者 Behrooz Maleki Hossein Keshvari Shirvan +1 位作者 Fereshteh Taimazi Elahe Akbarzadeh 《International Journal of Organic Chemistry》 2012年第1期93-99,共7页
Application of sulfuric acid immobilized on silica gel as an efficient and benign catalyst has been explored in the syn-thesis of 2,4,5-Triaryl-1H-imidazoles via condensation reaction of benzil or benzoin, aldehyde an... Application of sulfuric acid immobilized on silica gel as an efficient and benign catalyst has been explored in the syn-thesis of 2,4,5-Triaryl-1H-imidazoles via condensation reaction of benzil or benzoin, aldehyde and ammonium acetate. The key advantages of this process are high yields, cost effectiveness of catalyst, easy work-up, purification of products by non-chromatographic method and the reusability of the H2SO4.SiO2 catalyst. 展开更多
关键词 2 4 5-Trisubstituted IMIDAZOLES SOLVENT-FREE Synthesis multicomponent Reaction SILICA-SUPPORTED Sulfuric Acid Heterogeneous catalyst
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丙烷部分氧化制取丙烯醛Ⅰ.多组份氧化物催化剂的研究 被引量:9
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作者 杜鸿章 王贤高 +2 位作者 迟亚武 胡椒叶 李文钊 《石油化工》 CAS CSCD 北大核心 1997年第1期1-4,共4页
对丙烷氧化制取丙烯醛的多组份氧化物催化剂进行了制备研究和TPR、XRD表征。结果表明Bi-V-Mo-O与Bi-V-W-O催化剂对丙烷氧化制取丙烯醛具有较高的活性与选择性,Ag+是优良助剂。添加Ag+调变的Ag-Bi-... 对丙烷氧化制取丙烯醛的多组份氧化物催化剂进行了制备研究和TPR、XRD表征。结果表明Bi-V-Mo-O与Bi-V-W-O催化剂对丙烷氧化制取丙烯醛具有较高的活性与选择性,Ag+是优良助剂。添加Ag+调变的Ag-Bi-V-Mo-O催化剂在490℃、0.004MPa、3000ml/(gcath)条件下,丙烷转化率为46.9%,丙烯醛选择性为52.8%。TPR和XRD研究表明。 展开更多
关键词 多组份 氧化物催化剂 助剂 丙烯醛 丙烷部分氧化
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多元介孔混合氧化物La-Mn-Ce-O催化剂的制备与表征 被引量:11
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作者 刘咏 孟明 +1 位作者 姚金松 查宇清 《物理化学学报》 SCIE CAS CSCD 北大核心 2007年第5期641-646,共6页
采用柠檬酸络合-有机模板剂分解法制备出具有不同(n_(La)+n_(Mn))/(n_(La)+n_(Mn)+n_(Ce))比、不同温度焙烧的La-Mn-Ce-O系列多元介孔混合氧化物催化剂,并与传统共沉淀法制备的La-Mn-Ce-O催化剂进行比较.N_2吸附和脱附结果表明,采用模... 采用柠檬酸络合-有机模板剂分解法制备出具有不同(n_(La)+n_(Mn))/(n_(La)+n_(Mn)+n_(Ce))比、不同温度焙烧的La-Mn-Ce-O系列多元介孔混合氧化物催化剂,并与传统共沉淀法制备的La-Mn-Ce-O催化剂进行比较.N_2吸附和脱附结果表明,采用模板剂法制得的样品具有较大的比表面积(高达103.5m^2·g^(-1))和较均匀的孔径分布(3.4-4.4nm);500℃焙烧样品的比表面积约为共沉淀法所制样品的三倍.600℃焙烧后,样品的孔径分布范围稍有加宽,但仍保持介孔结构.XRD表征结果表明,Mn物种具有高度的分散性,XRD难以检测,La-Ce和Mn-Ce可能部分形成了固溶体结构.XPS结果揭示,Mn-Ce间存在电子态的强相互作用,出现了Mn2p的震激峰,这种相互作用促进了氧物种在Ce和Mn物种间的传递,增强了样品的氧化还原性能,震激峰最明显的样品具有最佳的氧化性能.H_2-TPR结果表明,采用柠檬酸络合-有机模板剂分解法制备的催化剂中,锰氧化物更容易被还原,Mn—O键的活动度与CO氧化活性密切相关.活性评价结果表明,500℃焙烧的(n_(La)+n_(Mn))/(n_(La)+n_(Mn)+n_(Ce))为0.5的样品,起燃温度比传统共沉淀法制得的样品降低了50℃左右,并表现出较高的热稳定性. 展开更多
关键词 多元介孔催化剂 制备 柠檬酸络合 有机模板剂 结构表征
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甲烷氧化偶联含锂多元复合氧化物催化剂的失活机理 被引量:3
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作者 远松月 赵震 +1 位作者 刘宝春 于作龙 《Chinese Journal of Catalysis》 SCIE CAS CSCD 北大核心 1995年第6期453-458,共6页
对甲烷氧化偶联反应活性较高的多元复合氧化物催化剂(Li-Ti-La.Li-Mn-La,Li-Ni-La)的稳定性和失活机理进行了初步探讨,利用XRD,IR,XPS和O2-TPD等方法对催化剂进行了表征.结果表明,催化... 对甲烷氧化偶联反应活性较高的多元复合氧化物催化剂(Li-Ti-La.Li-Mn-La,Li-Ni-La)的稳定性和失活机理进行了初步探讨,利用XRD,IR,XPS和O2-TPD等方法对催化剂进行了表征.结果表明,催化剂在高温及反应气氛的作用下,由于表面锂的流失,使体相晶格中的锂向表面扩散,导致含锂活性相结构的分解(或部分分解),从而减少了体相及表相氧空位和活性氧种的数量,降低了晶格氧的活动性,致使催化剂活性降低. 展开更多
关键词 甲烷 氧化偶联 多元氧化物 催化剂 失活机理
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过渡金属催化异腈参与的多组分反应研究进展 被引量:3
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作者 王也铭 刘兆洪 +1 位作者 唐春霖 毕锡和 《分子科学学报》 CAS CSCD 北大核心 2016年第1期1-19,共19页
综述介绍了近5年来过渡金属催化下异腈参与的多组分反应的研究进展.
关键词 异腈 多组分反应 过渡金属催化剂 插入反应 杂环化合物
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多组分Mo-Bi-Fe-O催化剂上丙烯氨氧化研究进展 被引量:4
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作者 安炜 《化学研究》 CAS 2002年第3期55-60,共6页
综述了多组分Mo_Bi_Fe_O催化剂上丙烯氨氧化研究进展 ,包括反应机理、催化剂设计、晶格氧迁移。
关键词 多组分Mo-Bi-Fe-O催化剂 选择性氧化 氨氧化 丙烯 丙烯腈 复合氧化物
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异丁烯两段催化氧化制甲基丙烯酸催化剂研究 Ⅰ.异丁烯气相氧化制甲基丙烯醛多元复合氧化物催化剂的研究 被引量:4
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作者 邱金恒 颜其洁 +1 位作者 傅献彩 佴如庆 《工业催化》 CAS 1994年第1期25-31,共7页
本文报导用于异丁烯(叔丁醇)选择氧化制MAL(甲基丙烯醛)的多元复合氧化物催化剂的研究结果。同共沉淀法制备的催化剂的活性主要决定于其化学组成,同时受到制备条件的影响。最佳催化剂的主要物相组成为PbO3,Bi2MoO3... 本文报导用于异丁烯(叔丁醇)选择氧化制MAL(甲基丙烯醛)的多元复合氧化物催化剂的研究结果。同共沉淀法制备的催化剂的活性主要决定于其化学组成,同时受到制备条件的影响。最佳催化剂的主要物相组成为PbO3,Bi2MoO3.3、NiMoO4、Sb2O3及a-Fe2O3小颗粒。在355℃,1000~2500h-1空速范围,叔丁醇:水:空气=1:3.3:7(摩尔比)的条件下可获得异丁烯转化率达96%,MAL选择性达89%的结果。 展开更多
关键词 异丁烯 甲基丙烯酸 催化剂 氧化
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Co/Si/Mo/Ni/Al_(2)O_(3)催化剂对汽油加氢脱硫性能的影响
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作者 田鑫 李欣 +2 位作者 王薇 吕鹏 马保军 《现代化工》 CAS CSCD 北大核心 2022年第7期130-134,140,共6页
为了研究活性组分的负载对催化剂加氢脱硫性能的影响,设计并制备了Co/Si/Mo/Ni/Al_(2)O_(3)多元复合催化剂。通过固定床催化剂评价装置对其进行二苯并噻吩加氢脱硫反应活性评价,并利用X射线衍射仪(XRD)、N_(2)吸附测试仪、X射线光电子... 为了研究活性组分的负载对催化剂加氢脱硫性能的影响,设计并制备了Co/Si/Mo/Ni/Al_(2)O_(3)多元复合催化剂。通过固定床催化剂评价装置对其进行二苯并噻吩加氢脱硫反应活性评价,并利用X射线衍射仪(XRD)、N_(2)吸附测试仪、X射线光电子能谱仪(XPS)、扫描电子显微镜(SEM)和Mapping等分析测试手段对催化剂进行表征。结果表明,复合催化剂具有优良的加氢脱硫性能,当活性组分负载量为(0.5%Co)/(1.5%Si)/(3.0%Mo)/(10.0%Ni)/Al_(2)O_(3)时,其加氢脱硫性能最高可达到96.1%。 展开更多
关键词 多元复合催化剂 加氢脱硫 固定床 二苯并噻吩 活性组分
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氢键活化的硝基烯参与的多组分不对称串联合成研究进展 被引量:3
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作者 严丽君 闫玉鑫 +1 位作者 陈雪冰 王永超 《有机化学》 SCIE CAS CSCD 北大核心 2020年第4期856-872,共17页
有机催化多组分不对称串联反应是构建复杂手性化合物的最有效方法之一,双功能手性催化剂是一类重要的单分子双活化有机小分子催化剂,能同时对多个反应底物进行氢键活化,实现多个新键的形成和多个手性中心的立体选择性控制.基于双功能催... 有机催化多组分不对称串联反应是构建复杂手性化合物的最有效方法之一,双功能手性催化剂是一类重要的单分子双活化有机小分子催化剂,能同时对多个反应底物进行氢键活化,实现多个新键的形成和多个手性中心的立体选择性控制.基于双功能催化剂氢键活化的硝基烯是一类重要的有机反应合成子,能参与多种有机小分子催化的串联反应.对硝基烯参与的多组分不对称串联反应,根据双功能催化剂的结构特征,从双功能硫脲-胺催化、双功能方酰胺-胺催化、其它双功能催化剂催化三个方面进行文献综述.从反应类型、反应机理、反应特点及应用等方面进行了系统地阐述,并对该领域的研究应用和发展前景进行了展望. 展开更多
关键词 双功能催化剂 氢键活化 硝基烯 多组分反应 不对称合成 串联反应
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