R. Galiasso, W. Garcia, M. M. Ramírez de Agudelo, P. Andréu
{"title":"Hydrotreatment of Cracked Light Gas Oil*","authors":"R. Galiasso, W. Garcia, M. M. Ramírez de Agudelo, P. Andréu","doi":"10.1201/9781315138886-7","DOIUrl":"https://doi.org/10.1201/9781315138886-7","url":null,"abstract":"","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"34 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114935904","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The Catalyzed Photodissociation of Water","authors":"G. Somorjai, M. Hendewerk, J. E. Turner","doi":"10.1080/01614948408064731","DOIUrl":"https://doi.org/10.1080/01614948408064731","url":null,"abstract":"Abstract Chemical interactions between molecules in excited electronic, vibrational, or rotational states and surfaces is a new field of catalytic science. Until recently, catalysis of chemical reactions has only been considered for molecules in their thermodynamic ground states. Most of the surface reactions to be catalyzed were exothermic or thermodynamically downhill. In carrying out endothermic reactions, the only source of energy considered has been the addition of heat. This also assured that the molecules maintained an equilibrium energy distribution throughout the reaction.","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"9 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123328483","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Fundamental Studies of Transition Metal Sulfide Hydrodesulfurization Catalysts","authors":"R. Chianelli","doi":"10.1080/01614948408064718","DOIUrl":"https://doi.org/10.1080/01614948408064718","url":null,"abstract":"Abstract Hydroprocessing catalysts based upon the transition metal sulfides have been widely used for over 60 years and catalysts such as Co/Mo/Al2O3 remain the industry “workhorses” in hydroprocessing of petroleum-based feedstocks [1]. Such applications include sulfur removal (hydrodesulfurization), nitrogen removal (hydrogenitrogenation), and product quality improvement (hydrotreating, hydroconversion). Original interest (prior to World War II) in these catalysts centered on their activityin the hydrogenation of coal liquids which contain considerable amounts of sulfur, thus maintaining the transition metal in the sulfided state. It was quickly discovered that Co, Ni, Mo, and W sulfides and their mixtures were the most active and least expensive of the transition metal sulfides [2]. Later (post-World War II) their major uses shifted to hydroprocessing of sulfur- and nitrogen-containing petroleum-based feedstocks with Co- and Ni-promoted Mo and W catalysts usually supported on Al2O3. However, as petroleu...","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"24 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121265576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Olefin Polymerization Catalysis Technology","authors":"H. Hsieh","doi":"10.1080/01614948408064729","DOIUrl":"https://doi.org/10.1080/01614948408064729","url":null,"abstract":"Abstract In the mid-1950s a series of patents on a new ethylene polymer was issued. These patents were all similar in that solid catalysts were used to produce polyethylene at relatively low ethylene pressures (Table 1). In contrast to the high pressure process which produced highly branched polymers with densities of 0.910 to 0.930 g/cm3, the new resins were linear and had densities of 0.940 to 0.970. Thus, the material made by the early ICI process became known as high pressure or low density (LDPE) polyethylene, and the new materials were called low pressure or high density (HDPE) polyethylene. This early technology for HDPE may be broadly grouped in terms of three different processes: Phillips, Standard Oil of Indiana, and Ziegler.","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129818566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Studies with High Activity Catalysts for Olefin Polymerization","authors":"F. Karol","doi":"10.1080/01614948408064726","DOIUrl":"https://doi.org/10.1080/01614948408064726","url":null,"abstract":"Abstract Catalysis continues to play a vital role in polymerization of such olefins as ethylene and propylene. A voluminous patent and scientific literature describing transition metal catalysts for olefin polymerization has emerged since the original discoveries by Ziegler, Natta, and other workers [1–6], Significant progress in polymerization catalysis has been made in the last 15 years, particularly with the development of methods to increase the efficiency of transition metal catalysts in olefin polymerization. Success in this area has provided the basis of simplified, less costly plant operations which do not require removal of residual catalyst from the polymer [3–9].","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"186 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126786115","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Methanol Conversion to Light Olefins","authors":"C. Chang","doi":"10.1080/01614948408064716","DOIUrl":"https://doi.org/10.1080/01614948408064716","url":null,"abstract":"Abstract Light olefins will play a dominant role in any future methanol-based chemicals economy. Olefins are initial products in the conversion of methanol to hydrocarbons over zeolite catalysts [1]. The overall reaction path may be represented by","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"597 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116071533","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Preparation and Properties of Fluid Cracking Catalysts for Residual Oil Conversion","authors":"J. Maselli, A. W. Peters","doi":"10.1080/01614948408064725","DOIUrl":"https://doi.org/10.1080/01614948408064725","url":null,"abstract":"Abstract Catalytic cracking of petroleum to produce gasoline began in about 1912. The early pioneering work was carried out by Eugene Houdry [1]. Modern fluid catalytic cracking (FCC) was conceived at Exxon and commercially developed in about 1940 [2] using amorphous catalysts. Fluid catalysts are small spherical particles ranging from 40 to 150 um in diameter with acid sites capable of cracking large petroleum molecules to products boiling in the gasoline range. One advantage of the FCC process is the absence of the diffusion limitations present in conventional gas oil cracking due to the small size of the catalyst particle. Since 1964 virtually all catalysts contain faujasite, a stable, large pore, Y-type zeolite dispersed in a silica/alumina matrix [3]. The catalytic aspects of contemporary FCC processes have been reviewed by Venuto and Habib [4], Gates, Katzer, and Schuit [5], Magee and Blazek [6], and Magee [7]. A more recent update of refinery trends has been made available by Blazek [8].","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122114366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The Present Status of Industrial Production and Use of Photovoltaic and Photocatalytic Solar Energy Conversion Devices","authors":"F. Wald","doi":"10.1080/01614948408064732","DOIUrl":"https://doi.org/10.1080/01614948408064732","url":null,"abstract":"Abstract The recent revival of interest in the direct use of solar energy, which followed the 1973 oil crisis, has brought increased research and development activity in a number of areas. Some of these areas are discussed here, namely photocatalysis, photoelectrochemical cells, and photovoltaic devices. At the present time there is continuing research activity in photocatalysis for various purposes, including solar energy conversion, and there is also continuing research activity in photoelectrochemical methods. However, at the present time, photovoltaic devices are the only ones in limited terrestrial application for direct solar energy conversion into electricity.","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"80 6","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"113981267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chemicals from Methanol","authors":"I. Wender","doi":"10.1080/01614948408064715","DOIUrl":"https://doi.org/10.1080/01614948408064715","url":null,"abstract":"Abstract For good reasons, there has been a spate of articles, much thinking, and a fair amount of industrial action on making chemicals and fuels from methanol, Only methane and methanol are made commercially in over 99% yields from synthesis gas.","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"21 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129321687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Novel Catalyst Geometry for Automobile Emission Control","authors":"C. Pereira, Gwan Kim, L. Hegedus","doi":"10.1080/01614948408064724","DOIUrl":"https://doi.org/10.1080/01614948408064724","url":null,"abstract":"Abstract The catalytic control of automobile exhaust pollutants (hydrocarbons, carbon monoxide, nitrogen oxides) is now a common practice in the United States and Japan, and there are strong indications that the technology may be introduced in other parts of the world in the coming years. The simultaneous conversion of all three of the above pollutants is achieved by the near-stoichiometric operation of noble metal catalysts which are supported either on alumina particles or on alumina-washcoated cordierite monoliths, A summary of the developments which lead to this technology can be found, e. g., in Hegedus and Gumbleton [1] and references therein.","PeriodicalId":253208,"journal":{"name":"Catalysis and Surface Science","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1984-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130310544","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}