Catalysts Catalyst deactivation

D.Y. (2006) Isomerization of n-butane to isobutane over Pt-modified beta and ZSM-5 zeolite catalyst catalyst deactivation and regeneration. Chem. Eng. ]., 120, 83-89. 

This was a Hquid-phase process which used what was described as siUceous zeoUtic catalysts. Hydrogen was not required in the process. Reactor pressure was 4.5 MPa and WHSV of 0.68 kg oil/h kg catalyst. The initial reactor temperature was 127°C and was raised as the catalyst deactivated to maintain toluene conversion. The catalyst was regenerated after the temperature reached about 315°C. Regeneration consisted of conventional controlled burning of the coke deposit. The catalyst life was reported to be at least 1.5 yr. 

Amorphous Silica—Alumina Based Processes. Amorphous siHca—alumina catalysts had been used for many years for xylene isomerization. Examples ate the Chevron (130), Mamzen (131), and ICI (132—135). The primary advantage of these processes was their simpHcity. No hydrogen was requited and the only side reaction of significance was disproportionation. However, in the absence of H2, catalyst deactivation via coking... 

Pure dry reactants are needed to prevent catalyst deactivation effective inhibitor systems are also desirable as weU as high reaction rates, since many of the specialty monomers are less stable than the lower alkyl acrylates. The alcohol—ester azeotrope (8) should be removed rapidly from the reaction mixture and an efficient column used to minimize reactant loss to the distillate. After the reaction is completed, the catalyst may be removed and the mixture distilled to obtain the ester. The method is particularly useful for the preparation of functional monomers which caimot be prepared by direct esterification. 

Hydrogenation of the oxides of carbon to methane according to the above reactions is sometimes referred to as the Sabatier reactions. Because of the high exothermicity of the methanization reactions, adequate and precise cooling is necessary in order to avoid catalyst deactivation, sintering, and carbon deposition by thermal cracking. 

Supported aqueous phase (SAP) catalysts (16) employ an aqueous film of TPPTS or similar ligand, deposited on a soHd support, eg, controlled pore glass. Whereas these supported catalysts overcome some of the principal limitations experienced using heterogeneous catalysts, including rhodium leaching and rapid catalyst deactivation, SAP catalysts have not found commercial appHcation as of this writing. 

Desalting is a water-washing operation performed at the production field and at the refinery site for additional cmde oil cleanup. If the petroleum from the separators contains water and dirt, water washing can remove much of the water-soluble minerals and entrained soflds. If these cmde oil contaminants are not removed, they can cause operating problems duting refinery processiag, such as equipment plugging and corrosion as well as catalyst deactivation. 

Because soHd acid catalyst systems offer advantages with respect to their handling and noncorrosive nature, research on the development of a commercially practical soHd acid system to replace the Hquid acids will continue. A major hurdle for soHd systems is the relatively rapid catalyst deactivation caused by fouling of the acid sites by heavy reaction intermediates and by-products. 

Eig. 1. Pathways for catalyst deactivation and ligand decomposition, where R = CgH. ... 

The Snamprogetti fluidized-bed process uses a chromium catalyst in equipment that is similar to a refinery catalytic cracker (1960s cat cracker technology). The dehydrogenation reaction takes place in one vessel with active catalyst deactivated catalyst flows to a second vessel, which is used for regeneration. This process has been commercialized in Russia for over 25 years in the production of butenes, isobutylene, and isopentenes. 

The appHcations of supported metal sulfides are unique with respect to catalyst deactivation phenomena. The catalysts used for processing of petroleum residua accumulate massive amounts of deposits consisting of sulfides formed from the organometaHic constituents of the oil, principally nickel and vanadium (102). These, with coke, cover the catalyst surface and plug the pores. The catalysts are unusual in that they can function with masses of these deposits that are sometimes even more than the mass of the original fresh catalyst. Mass transport is important, as the deposits are typically formed... 

In service, supported catalysts frequentiy undergo loss of activity over a period of time. In many cases, such catalyst deactivation is accompanied by the loss of accessible surface area of the active phase by sintering, by the accumulation of poisons, or by conversion of active sites to inactive species. 

The presence of other functional groups ia an acetylenic molecule frequendy does not affect partial hydrogenation because many groups such as olefins are less strongly adsorbed on the catalytic site. Supported palladium catalysts deactivated with lead (such as the Liadlar catalyst), sulfur, or quinoline have been used for hydrogenation of acetylenic compound to (predominantiy) cis-olefins. 

Catalyst lifetimes are long in the absence of misoperation and are limited primarily by losses to fines, which are removed by periodic sieving. Excessive operating temperatures can cause degradation of the support and loss of surface area. Accumulation of refractory dusts and chemical poisons, such as compounds of lead and mercury, can result in catalyst deactivation. Usually, much of such contaminants are removed during sieving. The vanadium in these catalysts may be extracted and recycled when economic conditions permit. 

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