首页 > 最新文献

Catalysis Reviews-Science and Engineering最新文献

英文 中文
The Different Catalytic Routes for Methane Valorization: An Assessment of Processes for Liquid Fuels 甲烷增值的不同催化途径:液体燃料过程的评估
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1993-06-01 DOI: 10.1080/01614949308014605
J. Fox
Abstract Scope of Review. This review is written from the point of view of the process design engineer trying to find the best catalytic options for upgrading methane. It is not intended to be a review of catalytic principles. In fact, actual catalysts used are only mentioned in passing. If the reader wishes to explore this aspect further, there are many recent review articles that can be used and these are referred to at an appropriate time and place.
摘要综述范围。这篇综述是从工艺设计工程师的角度出发,试图找到升级甲烷的最佳催化选择。这并不是对催化原理的回顾。实际上,实际使用的催化剂只是顺带提到的。如果读者希望进一步探讨这方面,可以使用许多最近的评论文章,并在适当的时间和地点参考这些文章。
{"title":"The Different Catalytic Routes for Methane Valorization: An Assessment of Processes for Liquid Fuels","authors":"J. Fox","doi":"10.1080/01614949308014605","DOIUrl":"https://doi.org/10.1080/01614949308014605","url":null,"abstract":"Abstract Scope of Review. This review is written from the point of view of the process design engineer trying to find the best catalytic options for upgrading methane. It is not intended to be a review of catalytic principles. In fact, actual catalysts used are only mentioned in passing. If the reader wishes to explore this aspect further, there are many recent review articles that can be used and these are referred to at an appropriate time and place.","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83578092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 200
Mechanistic Aspects of the Formation of Hydrocarbons and Alcohols from CO Hydrogenation 一氧化碳加氢生成碳氢化合物和醇的机理研究
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1993-02-01 DOI: 10.1080/01614949308013907
J. Hindermann, G. Hutchings, A. Kiennemann
Abstract In 1973 the oil crisis prompted considerable world interest in the production of synfuels which, as a result, led to the development of the Mobil Methanol to Gasoline Process [1] and more recently to the Shell Middle Distillate Process [2]. Synfuels have been a subject of both scientific and political interest for most of the 20th century. With the recent Gulf crisis, which has resulted in a surge in crude oil prices, it is clear that the search to find economic alternatives to the use of petroleum as an energy source will continue. This observation is based on the fact that the world reserves of coal and natural gas far exceed those of oil, and this fact alone implies that the conversion of coal and natural gas to transportation fuels is almost certain to become more widespread within the next 20 years.
1973年的石油危机引起了全世界对合成燃料生产的极大兴趣,这导致了美孚甲醇制汽油工艺的发展[1],以及最近壳牌中间馏分工艺的发展[2]。在20世纪的大部分时间里,合成燃料一直是科学和政治关注的主题。由于最近的海湾危机导致原油价格飙升,很明显,寻找石油作为能源的经济替代品的努力将继续下去。这一观察是基于这样一个事实,即世界上煤和天然气的储量远远超过石油的储量,而这一事实本身就意味着,在今后20年内,煤和天然气转化为运输燃料几乎肯定会变得更加普遍。
{"title":"Mechanistic Aspects of the Formation of Hydrocarbons and Alcohols from CO Hydrogenation","authors":"J. Hindermann, G. Hutchings, A. Kiennemann","doi":"10.1080/01614949308013907","DOIUrl":"https://doi.org/10.1080/01614949308013907","url":null,"abstract":"Abstract In 1973 the oil crisis prompted considerable world interest in the production of synfuels which, as a result, led to the development of the Mobil Methanol to Gasoline Process [1] and more recently to the Shell Middle Distillate Process [2]. Synfuels have been a subject of both scientific and political interest for most of the 20th century. With the recent Gulf crisis, which has resulted in a surge in crude oil prices, it is clear that the search to find economic alternatives to the use of petroleum as an energy source will continue. This observation is based on the fact that the world reserves of coal and natural gas far exceed those of oil, and this fact alone implies that the conversion of coal and natural gas to transportation fuels is almost certain to become more widespread within the next 20 years.","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1993-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89274548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 277
Transition metal ions in zeolites: siting and energetics of Cu2+ 沸石中的过渡金属离子:Cu2+的定位和能量学
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1993-01-01 DOI: 10.1080/01614949308013908
R. Schoonheydt
Abstract In this review only exchangeable cations on extralattice positions in zeolites are considered. Cu2+ is used as a probe for the siting, the nature, and the energy of the bonding to the lattice. The term zeolite encompasses the crystalline aluminosilicates and the crystalline aluminum phosphates (ALPO) with ion exchange and molecular sieving properties. However, exchangeable cations in isomorphously substituted ALPOs have not been studied systematically and are not treated here.
摘要本文只讨论沸石中晶格外位置的交换阳离子。Cu2+被用作定位、性质和与晶格键合能量的探针。沸石一词包括具有离子交换和分子筛分特性的结晶硅酸铝和结晶磷酸铝(ALPO)。然而,在同构取代的ALPOs中,交换阳离子尚未被系统地研究过,本文也不作讨论。
{"title":"Transition metal ions in zeolites: siting and energetics of Cu2+","authors":"R. Schoonheydt","doi":"10.1080/01614949308013908","DOIUrl":"https://doi.org/10.1080/01614949308013908","url":null,"abstract":"Abstract In this review only exchangeable cations on extralattice positions in zeolites are considered. Cu2+ is used as a probe for the siting, the nature, and the energy of the bonding to the lattice. The term zeolite encompasses the crystalline aluminosilicates and the crystalline aluminum phosphates (ALPO) with ion exchange and molecular sieving properties. However, exchangeable cations in isomorphously substituted ALPOs have not been studied systematically and are not treated here.","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82529181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 152
CO Oxidation and NO Reduction on Perovskite Oxides 钙钛矿氧化物的CO氧化和NO还原
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-12-01 DOI: 10.1080/01614949208016316
B. Viswanathan
Abstract The search for substitutes of noble metal supported exhaust control catalysts has led to the study of a number of perovskite oxides (1). The mechanisms of redox processes on these surfaces are topotactic in nature, thus accounting forthe reversible loss and uptake of bulk oxygen or for the concomitant creation and annihilation of vacancies rendering these systems as attractive oxidation catalysts. The variable oxygen stoichiometry of perovskite structure is responsible for the exotic behavior of these materials as a new class of high Tc superconducting oxides (2). The extreme ease of removing oxygen from the framework but still retaining the basic ingredients of the perovskite structure and the possibility of deriving different structural frameworks from ideal perovskite structure (e.g. insertion of rock salt layer between perovskite layers results in a K2NiF4 structure, while insertion of double [Bi2O2] layers between perovskite layers results in an Aurivillius phase) and the possibility of subs...
寻找贵金属支撑的废气控制催化剂的替代品已经导致了许多钙钛矿氧化物的研究(1)。这些表面上的氧化还原过程的机制本质上是拓扑性的,因此可以解释大量氧气的可逆损失和吸收,或者伴随的空位的产生和湮灭,使这些系统成为有吸引力的氧化催化剂。钙钛矿结构的可变氧化学测量是这些材料作为一类新的高Tc超导氧化物的奇特行为的原因(2)。从框架中极容易除去氧,但仍然保留了钙钛矿结构的基本成分,以及从理想的钙钛矿结构中衍生出不同结构框架的可能性(例如,在钙钛矿层之间插入岩盐层导致K2NiF4结构。而双[Bi2O2]层在钙钛矿层之间的插入会导致Aurivillius相)和subsubs的可能性。
{"title":"CO Oxidation and NO Reduction on Perovskite Oxides","authors":"B. Viswanathan","doi":"10.1080/01614949208016316","DOIUrl":"https://doi.org/10.1080/01614949208016316","url":null,"abstract":"Abstract The search for substitutes of noble metal supported exhaust control catalysts has led to the study of a number of perovskite oxides (1). The mechanisms of redox processes on these surfaces are topotactic in nature, thus accounting forthe reversible loss and uptake of bulk oxygen or for the concomitant creation and annihilation of vacancies rendering these systems as attractive oxidation catalysts. The variable oxygen stoichiometry of perovskite structure is responsible for the exotic behavior of these materials as a new class of high Tc superconducting oxides (2). The extreme ease of removing oxygen from the framework but still retaining the basic ingredients of the perovskite structure and the possibility of deriving different structural frameworks from ideal perovskite structure (e.g. insertion of rock salt layer between perovskite layers results in a K2NiF4 structure, while insertion of double [Bi2O2] layers between perovskite layers results in an Aurivillius phase) and the possibility of subs...","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83973287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 86
Reduction of Sulfur Dioxide on Perovskite Oxides 钙钛矿氧化物上二氧化硫的还原
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-12-01 DOI: 10.1080/01614949208016319
D. B. Hibbert
Abstract Reactions of sulfur dioxide on perovskite oxides have been investigated from two distinct standpoints. First sulfur dioxide is a poison for reactions of carbon monoxide, nitric oxide and hydrocarbons (1–11). How to mitigate this poisoning and how to regenerate the catalyst is therefore of importance when designing pollution abatement catalysts for motor cars. However the reaction between sulfur dioxide and carbon monoxide, catalyzed by perovskites, itself may provide an important route for the removal of a major pollutant (12–16).
从两个不同的角度研究了二氧化硫与钙钛矿氧化物的反应。首先,二氧化硫是一氧化碳、一氧化氮和碳氢化合物反应的毒药。因此,如何减轻这种中毒以及如何再生催化剂是设计汽车污染减排催化剂的重要问题。然而,由钙钛矿催化的二氧化硫和一氧化碳之间的反应本身可能为去除主要污染物提供重要途径(12-16)。
{"title":"Reduction of Sulfur Dioxide on Perovskite Oxides","authors":"D. B. Hibbert","doi":"10.1080/01614949208016319","DOIUrl":"https://doi.org/10.1080/01614949208016319","url":null,"abstract":"Abstract Reactions of sulfur dioxide on perovskite oxides have been investigated from two distinct standpoints. First sulfur dioxide is a poison for reactions of carbon monoxide, nitric oxide and hydrocarbons (1–11). How to mitigate this poisoning and how to regenerate the catalyst is therefore of importance when designing pollution abatement catalysts for motor cars. However the reaction between sulfur dioxide and carbon monoxide, catalyzed by perovskites, itself may provide an important route for the removal of a major pollutant (12–16).","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75027127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Decomposition of N2O on Perovskite-Related Oxides N2O在钙钛矿相关氧化物上的分解
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-12-01 DOI: 10.1080/01614949208016320
C. Swamy, J. Christopher
Abstract Mixed metal oxides crystalizing in a perovskite-related structure have long been of interest to solid state chemists and physicists because of their technologically important physical properties. The ready availability of a family of isomorphic solids with controllable physical properties makes these oxides suitable for basic research in catalysis. These mixed metal oxides are more advantageous and are better catalytic materials than simple oxides because: (i) the crystal structure can accomodate various metal ions and can stabilize unusual and mixed valence states of active metal ion; (ii) appropriate formulation of these oxides leads to easy tailoring of many desirable properties such as valence state of transition metal ion, distance between active sites, binding energy, diffusion of oxygen in the lattice, magnetic and conducting properties of the solid; (iii) the catalytic activity can be correlated to solid state properties since many of their solid state properties are thoroughly understood...
长期以来,以钙钛矿相关结构结晶的混合金属氧化物一直是固态化学家和物理学家的兴趣所在,因为它们在技术上具有重要的物理性质。一类具有可控物理性质的同构固体的现成可用性使这些氧化物适合用于催化的基础研究。这些混合金属氧化物比简单的氧化物更具优势,是更好的催化材料,因为:(1)晶体结构可以容纳多种金属离子,并能稳定活性金属离子的异常价态和混合价态;(ii)这些氧化物的适当配方可以很容易地调整许多理想的性质,如过渡金属离子的价态、活性位点之间的距离、结合能、氧在晶格中的扩散、固体的磁性和导电性;(iii)催化活性可以与固体性质相关联,因为它们的许多固体性质是完全了解的……
{"title":"Decomposition of N2O on Perovskite-Related Oxides","authors":"C. Swamy, J. Christopher","doi":"10.1080/01614949208016320","DOIUrl":"https://doi.org/10.1080/01614949208016320","url":null,"abstract":"Abstract Mixed metal oxides crystalizing in a perovskite-related structure have long been of interest to solid state chemists and physicists because of their technologically important physical properties. The ready availability of a family of isomorphic solids with controllable physical properties makes these oxides suitable for basic research in catalysis. These mixed metal oxides are more advantageous and are better catalytic materials than simple oxides because: (i) the crystal structure can accomodate various metal ions and can stabilize unusual and mixed valence states of active metal ion; (ii) appropriate formulation of these oxides leads to easy tailoring of many desirable properties such as valence state of transition metal ion, distance between active sites, binding energy, diffusion of oxygen in the lattice, magnetic and conducting properties of the solid; (iii) the catalytic activity can be correlated to solid state properties since many of their solid state properties are thoroughly understood...","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80493667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 66
Hydrogenation of Carbon Oxides over Perovskite-Type Oxides 钙钛矿型氧化物上碳氧化物的加氢反应
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-12-01 DOI: 10.1080/01614949208016315
J. Fierro
Abstract Transition metals, metal oxides and metal-containing mixed oxides have been extensively used for Fischer-Tropsch hydrocarbon synthesis (1–9) and their ability to yield oxygenated compounds. During the last two decades, an extensive search has been carried out in examining the mechanism of catalytic hydrogenation of co and CO, which produced hydrocarbons and oxygenate compounds. The catalytic models for hydrocarbon synthesis have already been reviewed by Vannice (lo), which gives detailed information and discusses the data which were obtained during their development. As a broad product distribution is obtained during the FT synthesis, the mechanisms are extremely complicated and not clearly understood: therefore this topic is beyond the objective of this chapter and hence no further attention will be paid.
过渡金属、金属氧化物和含金属的混合氧化物已广泛用于费托合成碳氢化合物(1-9)及其生成含氧化合物的能力。在过去的二十年中,人们对co和co催化加氢产生碳氢化合物和含氧化合物的机理进行了广泛的研究。Vannice (lo)对烃类合成的催化模型进行了综述,给出了详细的资料,并对其发展过程中获得的数据进行了讨论。由于FT合成过程中得到的产物分布很广,其机理极其复杂,不清楚,因此该主题超出了本章的目的,不再作进一步的关注。
{"title":"Hydrogenation of Carbon Oxides over Perovskite-Type Oxides","authors":"J. Fierro","doi":"10.1080/01614949208016315","DOIUrl":"https://doi.org/10.1080/01614949208016315","url":null,"abstract":"Abstract Transition metals, metal oxides and metal-containing mixed oxides have been extensively used for Fischer-Tropsch hydrocarbon synthesis (1–9) and their ability to yield oxygenated compounds. During the last two decades, an extensive search has been carried out in examining the mechanism of catalytic hydrogenation of co and CO, which produced hydrocarbons and oxygenate compounds. The catalytic models for hydrocarbon synthesis have already been reviewed by Vannice (lo), which gives detailed information and discusses the data which were obtained during their development. As a broad product distribution is obtained during the FT synthesis, the mechanisms are extremely complicated and not clearly understood: therefore this topic is beyond the objective of this chapter and hence no further attention will be paid.","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78467697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
Photocatalysis on Fine Powders of Perovskite Oxides 钙钛矿氧化物细粉的光催化性能
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-12-01 DOI: 10.1080/01614949208016318
T. Kutty, M. Avudaithai
Abstract Fine powders of semiconductor oxides have been widely used as photocatalysts for many reactions. Among the various photocatalytic reactions, water splitting has been given much importance, since it is a promising chemical route for solar energy conversion. Perovskite oxides, in particular SrTiO, have been commonly used as photocatalysts because some of them can decompose H,O into H, and 0, without an external bias potential (1). In turn, this is because the conduction band (CB) edges of some of the perovskite oxides are more negative than the H+/H, energy level. Since the catalytic activity is related to the surface properties of the solids, fine powders rather than single crystals are used. Photocatalysis on fine powers can be conveniently discussed in three parts, viz. preparation, characterization and their catalytic activity. Presently, photo-decomposition of water using SrTiO, fine powders is discussed in greater detail, although other photocatalytic reactions on various perovskite oxides ar...
摘要半导体氧化物的细粉末作为光催化剂已被广泛应用于许多反应。在各种光催化反应中,水裂解是一种很有前途的太阳能转化化学途径,受到了广泛的重视。钙钛矿氧化物,特别是SrTiO,通常被用作光催化剂,因为它们中的一些可以在没有外部偏置电位的情况下将H,O分解为H和0(1)。反过来,这是因为一些钙钛矿氧化物的导带(CB)边缘比H+/H,能级更负。由于催化活性与固体的表面性质有关,所以使用细粉末而不是单晶。细粉的光催化可以从制备、表征及其催化活性三个方面进行讨论。目前,使用SrTiO,细粉末对水的光分解进行了更详细的讨论,尽管在各种钙钛矿氧化物上的其他光催化反应尚不清楚。
{"title":"Photocatalysis on Fine Powders of Perovskite Oxides","authors":"T. Kutty, M. Avudaithai","doi":"10.1080/01614949208016318","DOIUrl":"https://doi.org/10.1080/01614949208016318","url":null,"abstract":"Abstract Fine powders of semiconductor oxides have been widely used as photocatalysts for many reactions. Among the various photocatalytic reactions, water splitting has been given much importance, since it is a promising chemical route for solar energy conversion. Perovskite oxides, in particular SrTiO, have been commonly used as photocatalysts because some of them can decompose H,O into H, and 0, without an external bias potential (1). In turn, this is because the conduction band (CB) edges of some of the perovskite oxides are more negative than the H+/H, energy level. Since the catalytic activity is related to the surface properties of the solids, fine powders rather than single crystals are used. Photocatalysis on fine powers can be conveniently discussed in three parts, viz. preparation, characterization and their catalytic activity. Presently, photo-decomposition of water using SrTiO, fine powders is discussed in greater detail, although other photocatalytic reactions on various perovskite oxides ar...","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74663321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Kinetics of Heterogeneous Catalyzed Reactions 非均相催化反应动力学
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-08-01 DOI: 10.1080/01614949208020307
Sol William Weller
Abstract The literature on heterogeneous catalytic kinetics is enormous, For this reason, the author has chosen to be selective rather than comprehensive. This review discusses, semihistorically and by reference to illustrative papers, the development of ideas and trends in research within the chosen topics. By way of warning: The author's interest in kinetics and chemisorption has been developing for some 50 years [1–6], One hopes that prejudices have softened over the years, but one knows they have not disappeared.
关于多相催化动力学的文献非常多,因此笔者选择了选择性而非全面性。这篇综述讨论,半历史和参考说明性的论文,在选定的主题研究的思想和趋势的发展。顺便提醒一下:作者对动力学和化学吸附的兴趣已经发展了大约50年[1-6],人们希望这些年来偏见已经软化,但人们知道它们并没有消失。
{"title":"Kinetics of Heterogeneous Catalyzed Reactions","authors":"Sol William Weller","doi":"10.1080/01614949208020307","DOIUrl":"https://doi.org/10.1080/01614949208020307","url":null,"abstract":"Abstract The literature on heterogeneous catalytic kinetics is enormous, For this reason, the author has chosen to be selective rather than comprehensive. This review discusses, semihistorically and by reference to illustrative papers, the development of ideas and trends in research within the chosen topics. By way of warning: The author's interest in kinetics and chemisorption has been developing for some 50 years [1–6], One hopes that prejudices have softened over the years, but one knows they have not disappeared.","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86344870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 40
Defects in Oxide Catalysts: Fundamental Studies of Catalysis in Action 氧化物催化剂的缺陷:作用催化的基础研究
IF 10.9 2区 化学 Q1 Chemistry Pub Date : 1992-02-01 DOI: 10.1080/01614949208021918
P. L. Gai-Boyes
Abstract Catalysis research underpins the science of modem chemical processing and fuel technologies. Catalysis is one of the most important technologies commercially in national economies. Solid-state heterogeneous catalyst materials such as metal oxides or metal particles on ceramic oxide substrates are most common. They are typically used with commodity gases and liquid reactants. Selective oxidation catalysis of hydrocarbon feedstocks is the dominant process converting them to key industrial chemicals, polymers, and energy sources, and is the basis of this review.
催化研究是现代化学加工和燃料技术的基础。催化是国民经济中最重要的商业化技术之一。固态非均相催化剂材料,如金属氧化物或陶瓷氧化物衬底上的金属颗粒是最常见的。它们通常用于商品气体和液体反应物。碳氢化合物原料的选择性氧化催化是将其转化为关键工业化学品、聚合物和能源的主要过程,也是本综述的基础。
{"title":"Defects in Oxide Catalysts: Fundamental Studies of Catalysis in Action","authors":"P. L. Gai-Boyes","doi":"10.1080/01614949208021918","DOIUrl":"https://doi.org/10.1080/01614949208021918","url":null,"abstract":"Abstract Catalysis research underpins the science of modem chemical processing and fuel technologies. Catalysis is one of the most important technologies commercially in national economies. Solid-state heterogeneous catalyst materials such as metal oxides or metal particles on ceramic oxide substrates are most common. They are typically used with commodity gases and liquid reactants. Selective oxidation catalysis of hydrocarbon feedstocks is the dominant process converting them to key industrial chemicals, polymers, and energy sources, and is the basis of this review.","PeriodicalId":50986,"journal":{"name":"Catalysis Reviews-Science and Engineering","volume":null,"pages":null},"PeriodicalIF":10.9,"publicationDate":"1992-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73487668","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 102
期刊
Catalysis Reviews-Science and Engineering
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1