Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Platinum surfaces methanation catalyst

Deng YQ, Neved TG, Ewen RJ, Honeybonme CL, Jones MG (1993) Sulfur poisoning, recovery and related phenomena over supported padadium, rhodiinn and iridium catalysts for methane oxidation. Appl Catal A 101 51-62 Ehrhardt JJ, CoUn L, Jamois D (1997) Poisoning of platinum surfaces by hexamethyldisdoxane (HMDS) application to catalytic methane sensors. Sens Actuators B 40 117-124 Firth JG, Jones A, Jones TA (1973) The principles of the detection of flammable atmospheres by catalytic devices. Combust Flame 21 303-311... [Pg.291]

During the reaction of the hot catalyst surface with a flammable gas the temperature of the device increases. The Platinum coil itself serves at the same time as a resistance thermometer. The resistance increase of the coil then is a direct measure for the amount of combusted gas. Usually the amount of heat that develops during combustion is small and amounts to 800 kj/mol for methane, for example [8], Therefore the sensor is connected in a bridge circuit to a second resistor which shows the same setup as the pellistor but is catalytically inactive. The bridge voltage is then controlled by the temperature difference of the two sensors (see Fig. 5.34). [Pg.144]

Nickel-platinum bimetallic catalysts showed higher activity during ATR than nickel and platinum catalysts blended in the same bed. It was hypothesized that nickel catalyzes SR, whereas platinum catalyzes POX and, when they are added to the same support, the heat transfer between the two sites is enhanced [59, 60]. Advanced explanations were reported by Dias and Assaf [60] in a study on ATR of methane catalyzed by Ni/y-Al203 with the addition of small amounts of Pd, Pt or Ir. An increase in methane conversion was observed, ascribed to the increase in exposed Ni surface area favored by the noble metal under the reaction conditions. [Pg.296]

To date, the only shock tube apparatus equipped to study surface reactions is the KIST facility at ATK GASL in New York. The tests done so far have studied methane oxidation, CFI4 + 2O2 CO2 + 2H2O on the surface of an SCT ferrous-based reactor impregnated with platinum based catalyst. To isolate the effects of the screen and the catalyst on the reaction, three types of tests were run catalyzed screen with combustible gases,... [Pg.211]

Attempts have been made to mimic proposed steps in catalysis at a platinum metal surface using well-characterized binuclear platinum complexes. A series of such complexes, stabilized by bridging bis(diphenyl-phosphino)methane ligands, has been prepared and structurally characterized. Included are diplati-num(I) complexes with Pt-Pt bonds, complexes with bridging hydride, carbonyl or methylene groups, and binuclear methylplatinum complexes. Reactions of these complexes have been studied and new binuclear oxidative addition and reductive elimination reactions, and a new catalyst for the water gas shift reaction have been discovered. [Pg.232]

A convenient method to produce porous surfaces is the anodic oxidation of aluminum plates. Such microstructured aluminum platelets have been coated by wet impregnation with Pt-, V- and Zr-precursors [35], and tested under catalytic methane combustion conditions. The conversion rate of oxygen followed directly the platinum content in the catalysts. These data were well reproducible even after five different runs. [Pg.99]

The results show that the specificities of catalyst deactivation and it s kinetic description are in closed connection with reaction kinetics of main process and they form a common kinetic model. The kinetic nature of promotor action in platinum catalysts side by side with other physicochemical research follows from this studies as well. It is concern the increase of slow step rate, the decrease of side processes (including coke formation) rate and the acceleration of coke transformation into methane owing to the increase of hydrogen contents in coke. The obtained data can be united by common kinetic model.lt is desirable to solve some problems in describing the catalyst deactivation such as the consideration of coke distribution between surfaces of metal, promoter and the carrier in the course of reactions, diffusion effects etc,. [Pg.548]


See other pages where Platinum surfaces methanation catalyst is mentioned: [Pg.355]    [Pg.224]    [Pg.519]    [Pg.22]    [Pg.41]    [Pg.204]    [Pg.62]    [Pg.460]    [Pg.331]    [Pg.331]    [Pg.98]    [Pg.122]    [Pg.32]    [Pg.22]    [Pg.88]    [Pg.172]    [Pg.409]    [Pg.293]    [Pg.348]    [Pg.62]    [Pg.105]    [Pg.151]    [Pg.512]    [Pg.128]    [Pg.242]    [Pg.485]    [Pg.244]    [Pg.112]    [Pg.120]    [Pg.139]    [Pg.172]    [Pg.220]    [Pg.88]    [Pg.122]    [Pg.136]    [Pg.147]    [Pg.7]    [Pg.177]    [Pg.178]    [Pg.418]    [Pg.315]    [Pg.164]    [Pg.640]    [Pg.10]   
See also in sourсe #XX -- [ Pg.28 ]




SEARCH



Catalysts methane

Methanation Catalyst

Platinum methanation catalyst

Platinum methane

Platinum surfaces

Platinum surfaces methanation

Surface catalysts

© 2024 chempedia.info