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A Spectroscopic Study of Methane Oxidative Coupling Catalysts

A Spectroscopic Study of Methane Oxidative Coupling Catalysts PDF Author: Xueming Yang
Publisher:
ISBN:
Category :
Languages : en
Pages : 258

Book Description


A Spectroscopic Study of Methane Oxidative Coupling Catalysts

A Spectroscopic Study of Methane Oxidative Coupling Catalysts PDF Author: Xueming Yang
Publisher:
ISBN:
Category :
Languages : en
Pages : 258

Book Description


A Study of Catalysts for the Oxidative Coupling of Methane

A Study of Catalysts for the Oxidative Coupling of Methane PDF Author: Y. Tsuru
Publisher:
ISBN:
Category :
Languages : en
Pages : 16

Book Description


Diffuse Reflectance Fourier Transform Infrared Spectroscopy and Transient Studies of Oxidative Coupling of Methane Over Li/MgO Catalyst

Diffuse Reflectance Fourier Transform Infrared Spectroscopy and Transient Studies of Oxidative Coupling of Methane Over Li/MgO Catalyst PDF Author: Soujanya Chidanand Bhumkar
Publisher:
ISBN:
Category : Catalysts
Languages : en
Pages : 284

Book Description


Methane Conversion by Oxidative Processes

Methane Conversion by Oxidative Processes PDF Author: Wolf
Publisher: Springer Science & Business Media
ISBN: 9401574499
Category : Technology & Engineering
Languages : en
Pages : 556

Book Description
A reasonable case could be made that the scientific interest in catalytic oxidation was the basis for the recognition of the phenomenon of catalysis. Davy, in his attempt in 1817 to understand the science associated with the safety lamp he had invented a few years earlier, undertook a series of studies that led him to make the observation that a jet of gas, primarily methane, would cause a platinum wire to continue to glow even though the flame was extinguished and there was no visible flame. Dobereiner reported in 1823 the results of a similar investigation and observed that spongy platina would cause the ignition of a stream of hydrogen in air. Based on this observation Dobereiner invented the first lighter. His lighter employed hydrogen (generated from zinc and sulfuric acid) which passed over finely divided platinum and which ignited the gas. Thousands of these lighters were used over a number of years. Dobereiner refused to file a patent for his lighter, commenting that "I love science more than money." Davy thought the action of platinum was the result of heat while Dobereiner believed the ~ffect ~as a manifestation of electricity. Faraday became interested in the subject and published a paper on it in 1834; he concluded that the cause for this reaction was similar to other reactions.

Study of the Oxidative Coupling Reaction of Methane on Solid Basic Catalysts

Study of the Oxidative Coupling Reaction of Methane on Solid Basic Catalysts PDF Author: G. Zu
Publisher:
ISBN:
Category :
Languages : en
Pages : 11

Book Description


Methane Conversion

Methane Conversion PDF Author: D.M. Bibby
Publisher: Elsevier
ISBN: 0080960707
Category : Technology & Engineering
Languages : en
Pages : 759

Book Description
This proceedings volume comprises the invited plenary lectures, contributed and poster papers presented at a symposium organised to mark the successful inauguration of the world's first commercial plant for production of gasoline from natural gas, based on the Mobil methanol-to-gasoline process. The objectives of the Symposium were to present both fundamental research and engineering aspects of the development and commercialization of gas-to-gasoline processes. These include steam reforming, methanol synthesis and methanol-to-gasoline. Possible alternative processes e.g. MOGD, Fischer-Tropsch synthesis of hydrocarbons, and the direct conversion of methane to higher hydrocarbons were also considered.The papers in this volume provide a valuable and extremely wide-ranging overview of current research into the various options for natural gas conversion, giving a detailed description of the gas-to-gasoline process and plant. Together, they represent a unique combination of fundamental surface chemistry catalyst characterization, reaction chemistry and engineering scale-up and commercialization.

The Oxidative Coupling of Methane by Metal Oxides and Phosphates

The Oxidative Coupling of Methane by Metal Oxides and Phosphates PDF Author: Robert Lawrence Tatterson
Publisher:
ISBN:
Category :
Languages : en
Pages : 284

Book Description


Methane and Alkane Conversion Chemistry

Methane and Alkane Conversion Chemistry PDF Author: M.M. Bhasin
Publisher: Springer Science & Business Media
ISBN: 1461518075
Category : Science
Languages : en
Pages : 338

Book Description
Natural gas, an abundant natural energy and chemical resource, is underutilized. Its inherent high energy content is compromised by its volatility. Storage and transportation problems abound for liquified natural gas. Several of the drawbacks of the utilization of natural gas, particularly its high volatility, could be offset by development of an economical and efficient process for coupling and/or further homologation of its principal component, methane. Alternatively, other conversion strategies such as partial oxidation to methanol and syngas, to oxygenates or conversion to such products via the intermediacy of chlorides should also be considered. Given the energy-intensive regimes necessary for the likely activation of methane, it was inevitable that researchers would tum to the use of heterogeneous catalysts. Heterogeneous catalysis is now a relatively mature discipline with numerous and diverse reactions being explored alongside informative studies on surface characterization, mechanism, and theory. Relationships to important related areas such as homogeneous catalysis, organometallic chemistry, and inorganic chemistry have become firmly established within this discipline. The field of methane and alkane activation is now over ten years old. The first decade of investigation produced results plagued by low yields and low-moderate conversions with well-articulated mechanistic limitations. As we begin the second decade of inquiry, novel strategies have brought increasing yields and conversions to such products as ethane, ethylene, methanol, and formaldehyde. These new approaches utilize separation of products via membranes or adsorbents. Moreover, additional mechanistic insight has been forthcoming from theoretical and computational examination as well as experimental investigation.

Alternative Energies

Alternative Energies PDF Author: Germán Ferreira
Publisher: Springer Science & Business Media
ISBN: 3642406807
Category : Technology & Engineering
Languages : en
Pages : 286

Book Description
This book presents nine chapters based on fundamental and applied research of alternative energies. At the present time, the challenge is that technology has to come up with solutions that can provide environmentally friendly energy supply options that are able to cover the current world energy demand. Experts around the world are working on these issues for providing new solutions that will break the existing technological barriers. This book aims to address key pillars in the alternative energy field, such as: biomass energy, hydrogen energy, solar energy, wind energy, hydroelectric power, geothermal energy and their environmental implications, with the most updated progress for each pillar. It also includes the life cycle assessment (LCA) and thermoeconomic analysis (TA) as tools for evaluating and optimising environmental and cost subjects. Chapters are organized into fundamental research, applied research and future trends; and written for engineers, academic researches and scientists.

Catalytic Conversion of Carbon Monoxide and Methane Over Metal and Metal Oxide Catalysts

Catalytic Conversion of Carbon Monoxide and Methane Over Metal and Metal Oxide Catalysts PDF Author: Wenchi Liu
Publisher:
ISBN:
Category :
Languages : en
Pages : 93

Book Description
Catalysis is of vital importance in a wide range of areas including energy processing and chemical production. Catalytic conversion of C1 sources such as carbon monoxide and methane to make hydrocarbon fuels and oxygenated products has far reaching implications especially in the context of the gradual depletion of crude oil resource and the potential surge in the natural gas production in the coming decades. The control over reaction activity and selectivity for the conversion CO and CH4 in the Fischer–Tropsch synthesis and oxidative coupling of methane (OCM) have received tremendous attention and have been proved challenging. This dissertation focuses on the catalytic conversion of CO (Fischer–Tropsch synthesis) using supported cobalt based bimetallic nanoparticle model catalysts and the oxidative coupling of methane with noble metal promoted metal oxide catalysts. Using colloidal synthesis, a series of cobalt based bimetallic nanoparticles Co–M (M = Mn, Ru, Rh, and Re) with well-defined sizes, shapes, and compositions were obtained. Detailed synthesis procedures were presented and key synthetic parameters were discussed. The as-synthesized nanoparticles were subjected to extensive in-situ X-ray spectroscopy studies using ambient pressure X-ray photoelectron spectroscopy (AP-XPS) and X-ray absorption spectroscopy (XAS) under catalytic relevant conditions. Composition wise, the results indicate the surface concentration of Co on the as-synthesized Co–M bimetallic particles is slightly less than the bulk atomic Co %. While oxidation treatment led to a slight increase of the surface Co, major effect was seen after the reduction treatment where surface segregation of the second metal resulted in a drastic decrease of the surface Co content. The effect is more pronounced at elevated reduction temperatures. Under reaction conditions, the surface compositions remained similar to those after the reduction treatment at high temperatures. Among the bimetallics tested, the Co–Mn system is relatively less susceptible to surface reconstructions induced by oxidation and reduction treatments. In addition, the reducibility of Co was also shown to be modified depending on the second metal present and Re was proved to be most efficient in leading to a facile reduction of Co. Catalytic performance of the bimetallic catalysts supported on mesoporous silica MCF–17 indicates a positive effect in the catalytic activity for Co–Rh and Co–Mn systems, while Co–Re and Co–Cu showed decreased activity. Less pronounced promotion effect of the second metal on the product distribution was observed with only a slight increase in the selectivity towards C5+ products. The selectivities for CH4 and C5+ of the various Co–M bimetallic catalysts generally resemble those of pure Co catalysts. Although in extremely low selectivity, alcohols were also formed with Co–Rh and Co–Cu bimetallic catalysts. The appearance of longer chain alcohol such as propanol, which was not present for pure Co catalysts, is an evidence for potential synergistic promotion. For oxidative coupling of methane (OCM), the promotion effect of noble metals (Pt, Ir, and Rh) on the performance of MnxOy-Na2WO4/MCF–17 catalysts was investigated. The introduction of noble metals had little effect on the surface area and phase composition of the original catalyst but led to a more reduced nature of the surface oxide species. Catalytic study revealed an enhanced selectivity towards both C2 and C3 hydrocarbons as compared to the undoped MnxOy-Na2WO4/MCF–17 catalyst in the order of Rh-doped > Ir-doped > Pt-doped samples together with a lower olefin to paraffin ratio. A more optimized strength of interaction between the carbon intermediates and the catalyst surface was suggested, which in combination with the improved reducibility of Mn and W species are believed to be responsible for the improved performance. In addition, monodispersed leaf-like manganese–tungsten–oxide (Mn–W–Ox) nanoparticles and hydroxylated hexagonal boron nitride (h-BN) were synthesized and used as novel catalysts in OCM reaction. Preliminary results indicate that the MCF–17 supported Mn–W–Ox nanoparticle catalyst showed a CH4 conversion of 5.4% and C2 selectivity of 42% with good stability over time. On the other hand, hydroxylated h-BN exhibited good activity (~20% CH4 conversion) with moderate selectivity towards C2 hydrocarbons (20%–30%). However, the hydroxylated h-BN catalysts faced serious deactivation, which was not eliminated by lowering the reaction temperature or the oxygen concentration in the reaction gas feed.