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Reaction dehydrogenation

Finely divided palladium is a good catalyst and is used for hydrogenation and dehydrogenation reactions. It is alloyed and used in jewelry trades. [Pg.112]

Dehydrogenation processes for acetone, methyl isobutyl ketone [108-10-1], and higher ketones (qv) utilizing, in one process, a copper-based catalyst have been disclosed (18,19). Dehydrogenation reaction is used to study the acid—base character of catalytic sites on a series of oxides (20,21). [Pg.105]

Sobering investigators uncovered a second significant breakthrough in microbial biotechnology of steroid production. They discovered that Corynebacterium simplex converted hydrocortisone (cortisol) (29) to prednisolone via a 1,2-dehydrogenation reaction. This A -3-ketosteroid is a highly active antiinflammatory commercial product (162). [Pg.430]

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. [Pg.368]

Although this pure dehydrogenation reaction is not practiced commercially, at least two processes exist in which methanol is dehydrogenated to formaldehyde in the presence of air. [Pg.198]

Deposition reactions for some reducing agents are given in Table 1 hydrogen is a principal by-product of each reduction. Elemental phosphoms or boron is codeposited with the reduced metal from hypophosphite, borohydride, or organoborane baths (15). Other minor reactions can also occur (18). All of these reductions can be viewed as dehydrogenation reactions (16,19). [Pg.107]

Membrane Reactor. Another area of current activity uses membranes in ethane dehydrogenation to shift the ethane to ethylene equiUbrium. The use of membranes is not new, and has been used in many separation processes. However, these membranes, which are mostly biomembranes, are not suitable for dehydrogenation reactions that require high temperatures. Technology has improved to produce ceramic and other inorganic (90) membranes that can be used at high temperatures (600°C and above). In addition, the suitable catalysts can be coated without blocking the pores of the membrane. Therefore, catalyst-coated membranes can be used for reaction and separation. [Pg.443]

The dehydrogenation reaction produces crude styrene which consists of approximately 37.0% styrene, 61% ethylbenzene and about 2% of aromatic hydrocarbon such as benzene and toluene with some tarry matter. The purification of the styrene is made rather difficult by the fact that the boiling point of styrene (145.2°C) is only 9°C higher than that of ethylbenzene and because of the strong tendency of styrene to polymerise at elevated temperatures. To achieve a successful distillation it is therefore necessary to provide suitable inhibitors for the styrene, to distil under a partial vacuum and to make use of specially designed distillation columns. [Pg.428]

The dehydrogenation reaction is an extremely rapid endothermic reaction which converts alkylcyclohexanes to aromatics almost quantitatively. It is promoted by the catalyst platinum function and is so rapid that it is normally limited by diffusion into the catalyst particle. [Pg.48]

The simplest paraffin (alkane) and the most widely used feedstock for producing ethylene is ethane. As mentioned earlier, ethane is obtained from natural gas liquids. Cracking ethane can be visualized as a free radical dehydrogenation reaction, where hydrogen is a coproduct ... [Pg.91]

The dehydrogenation reaction is carried out using either copper or zinc oxide catalyst at approximately 450-550°C. A 95% yield is obtained ... [Pg.229]

The oxidation process uses air as the oxidant over a silver or copper catalyst. The conditions are similar to those used for the dehydrogenation reaction. [Pg.230]

Dehydrogenation of ethylbenzene to styrene occurs over a wide variety of metal oxide catalysts. Oxides of Ee, Cr, Si, Co, Zn, or their mixtures can be used for the dehydrogenation reaction. Typical reaction... [Pg.266]

Metals are most active when they first deposit on the catalyst. With time, they lose their initial effectiveness through continuous oxidation-reduction cycles. On average, about one third of the nickel on the equilibrium catalyst will have the activity to promote dehydrogenation reactions. [Pg.64]

Catalyst composition and feed chloride have a noticeable impact on hydrogen yield. Catalysts with an active alumina matrix tend to increase the dehydrogenation reactions. Chlorides in the feed reactivate aged nickel, resulting in high hydrogen yield. [Pg.64]

The HVCH ratio is an indicator of dehydrogenation reactions. However, the ratio is sensitive to the reactor temperature and the type of catalyst. A better indicator of nickel activity is the volume of... [Pg.64]

Vanadium also promotes dehydrogenation reactions, but less than nickel. Vanadium s contribution to hydrogen yield is 20% to 50% of nickel s contribution, but vanadium is a more severe poison. Unlike nickel, vanadium does not stay on the surface of the catalyst. Instead, it migrates to the inner (zeolite) part of the catalyst and destroys the zeolite crystal structure. Catalyst surface area and activity are permanently lost. [Pg.65]

These metals, when deposited on the E-cat catalyst, increase coke and gas-making tendencies of the catalyst. They cause dehydrogenation reactions, which increase hydrogen production and decrease gasoline yields. Vanadium can also destroy the zeolite activity and thus lead to lower conversion. The deleterious effects of these metals also depend on the regenerator temperature the rate of deactivation of a metal-laden catalyst increases as the regenerator temperature increases. [Pg.108]

The effects of antimony passivation are usually immediate. By forming an alloy with nickel, the dehydrogenation reactions that are... [Pg.122]

Dehydrogenation. Under ideal conditions (i.e., a clean feedstock and a catalyst with no metals), cat cracking does not yield any appreciable amount of molecular hydrogen. Therefore, dehydrogenation reactions will proceed only if the catalyst is contaminated with metals such as nickel and vanadium. [Pg.135]

Flavin Adenine Dinucleotide (FAD) (C27 H33 N9 O15P2) is a coenzyme that acts as a hydrogen acceptor in dehydrogenation reactions in an oxidized or reduced form. FAD is one of the primary cofactors in biological redox reactions. [Pg.507]

P/Pd denotes the ratio pNC/Pc3n6 or PncSPco The p0, range isO-6 kPa. Hydrogenation and dehydrogenation reactions. ... [Pg.160]

The first example of a neutral aluminum complex of diazaphosphane, the 1,3,2,4-diazaphosphaluminetidine 50, Eq. (4), has been synthesized by the dehydrogenation reaction between Lewis acid-base adduct H3AI <— NMca and fBuP[N(H)fBu 2 49. The product fBuP(NfBu)2(H)Al [Pg.111]

Suleimenov and Ha have used high-level G2 and CBS-Q ab initio methods to study the thermochemical properties of gaseous polysulfanes (H2S , =l-6) [4]. The enthalpy of formation were calculated from atomisation energies and from enthalpies of dehydrogenation reactions such as shown in Eq. (1) ... [Pg.9]

Example 7.9 Determine AHji for the ethylbenzene dehydrogenation reaction at 973 K and 0.5 atm. [Pg.234]


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Activated dehydrogenation reactions

Activated dehydrogenative coupling reactions

Alkane dehydrogenations reaction

Alkyl halides, 787 dehydrogenation reactions

Assisted Cross-Dehydrogenative-Coupling Reactions

Carbon dehydrogenation reactions

Catalytic reactions dehydrogenation

Catalytic reactions dehydrogenative coupling

Chemical reactions dehydrogenation

Copper-catalyzed cross-dehydrogenative coupling reactions

Dehydrogenation Mechanism and Gas-Phase HO)-Dependent Elementary Reactions

Dehydrogenation and rehydrogenation reactions

Dehydrogenation and rehydrogenation reactions in alanates

Dehydrogenation reaction 269 equilibrium constant

Dehydrogenation reaction conditions

Dehydrogenation reactions dense metallic membrane

Dehydrogenation reactions of flavoproteins, table

Dehydrogenation reactions reactors

Dehydrogenation reactions zeolite membrane reactors

Dehydrogenation/isomerization reaction

Dehydrogenations reaction velocity

Dehydrogenations reactions

Dehydrogenations reactions

Dehydrogenative Coupling Reactions

Dehydrogenative Heck-type reactions

Dehydrogenative cross-coupling reactions

Dehydrogenative silylation reactions

Elimination reactions dehydrogenation of alkanes

Elimination reactions dehydrogenative silane

Flavoprotein dehydrogenation reactions

Generalized Reaction Scheme for Oxidative Dehydrogenation of Alkanes

Graphitic dehydrogenation reactions

Hammett equation for dehydrogenation reactions

Hydrocarbon reactions cyclohexane dehydrogenation

Hydrogen-Transfer and Dehydrogenation Reactions

Hydrogen-permeable membrane dehydrogenation reaction

Hydrogenation/Dehydrogenation reactions

In hydrogenation-dehydrogenation reactions

Iridium-catalyzed dehydrogenation reaction conditions

Iridium-catalyzed dehydrogenation transfer reaction

Lactones, a-methylenesynthesis via dehydrogenation reactions

Membrane reactors dehydrogenation reactions

Methane Steam Reforming and Dehydrogenation Reactions

Methanol, reaction dehydrogenation

Olefin Syntheses by Dehydrogenation and Other Elimination Reactions

Oligomerization/dehydrogenation reaction

Oxidation reactions, alkene oxidative dehydrogenation

Oxidative dehydrogenation reactions

Palladium-based membranes dehydrogenation reactions

Pericyclic reactions dehydrogenation

Photocatalytic reactions dehydrogenation

Platinum dehydrogenation reactions

Platinum dehydrogenation reactions cyclohexane

Platinum dehydrogenation reactions other

Porous ceramic membranes dehydrogenation reaction

Reaction kinetics isobutane dehydrogenation

Reaction rate constant, dehydrogenation

Reaction scheme dehydrogenation

Reactions alcohols, dehydrogenation

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