Big Chemical Encyclopedia

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

Articles Figures Tables About

Hydrogen normalization

Some processes use only one reactor (57) or a combination of liquid- and vapor-phase reactors (58). The goal of these schemes is to reduce energy consumption and capital cost. Hydrogenation normally is carried out at 2—3 MPa (20—30 atm). Temperature is maintained at 300—350°C to meet a typical specification of less than 500 ppm benzene in the product at higher temperatures, thermodynamic equiUbrium shifts to favor benzene and the benzene specification is impossible to attain. Also, at higher temperatures, isomerization of cyclohexane to methylcyclopentane occurs typically there is a 200 ppm specification limit on methylcyclopentane content. [Pg.408]

The formation of 33 in the case of 32 can be explained by attack of some of the CCI2 ipso to the CH3 group. Since this position does not contain a hydrogen, normal proton loss cannot take place and the reaction ends when the CCli" moiety acquires a proton. [Pg.717]

For a review of Raney nickel, see Pizey, J.S. Ref. 166, vol. 2, p. 175. Double bonds have been reduced with Raney nickel alone with no added H2. The hydrogen normally present in this reagent was sufficient Pojer, P.M. Chem. Ind. (London), 1986, 177. [Pg.1107]

The steam reforming of natural gas process is the most economic near-term process among the conventional processes. On the other hand, the steam reforming natural gas process consists of reacting methane with steam to produce CO and H2. The CO is further reacted or shifted with steam to form additional hydrogen and CO2. The CO2 is then removed from the gas mixture to produce a clean stream of hydrogen. Normally the CO2 is vented into the atmosphere. For decarbonization, the CO2 must be sequestered[l,2]. The alternative method for hydrogen production with sequestration of carbon is the thermal decomposition of methane. [Pg.421]

How many covalent bonds will carbon normally form in a compound How many covalent bonds will hydrogen normally form in a compound ... [Pg.170]

An augmented central composite design was used in obtaining reaction-rate data in a flow differential reactor the reaction occurring was the isomerization of normal pentane to isopentane in the presence of hydrogen (Cl). Using the subscripts 1, 2, and 3 for hydrogen, normal pentane, and isopentane respectively, an empirical rate equation can be written... [Pg.156]

Deuterium An isotope of hydrogen whose nucleus contains one neutron and one proton, thus making it nearly twice as heavy as the nucleus of normal hydrogen (normal hydrogen has a single proton). This material is commonly referred to as heavy hydrogen. It occurs naturally as 1 atom to 6,500 atoms of normal hydrogen and is not radioactive. [Pg.231]

Benzoquinone. The formation of cyanocobaltate(II) in a hydrogen atmosphere and in the presence of excess benzoquinone resulted in the absorption of only 40% of that amount of hydrogen normally taken up in the formation of CoH, and the substrate was not catalytically reduced addition of alkali did not activate the system. When excess benzoquinone was added to CoH (H2 atmosphere), hydrogen was not absorbed and, again, alkali did not activate the system. The addition of less than stoichiometric quantities of substrate also resulted in no hydrogen absorption. [Pg.215]

Helium-4 Para-hydrogen Normal Hydrogen Nitrogen Oxygen Argon Carbon Dioxide Acetylene Methane... [Pg.1216]

Figure 13.12. The thymidylate synthase reaction, and its inhibition by 5-fluoro-deoxyuridinemonophosphate (5-FdUMP). a Overview of the reaction, b The catalytic mechanism. The enzyme forms an intermediate in which it is covalently linked to both the substrate (UMP) and, via the latter, to the coenzyme (bottom center). Resolution of this intermediate does not happen with 5-FdUMP because it requires abstractionof the hydrogen normally found in position 5 of the uracil ring. Figure 13.12. The thymidylate synthase reaction, and its inhibition by 5-fluoro-deoxyuridinemonophosphate (5-FdUMP). a Overview of the reaction, b The catalytic mechanism. The enzyme forms an intermediate in which it is covalently linked to both the substrate (UMP) and, via the latter, to the coenzyme (bottom center). Resolution of this intermediate does not happen with 5-FdUMP because it requires abstractionof the hydrogen normally found in position 5 of the uracil ring.
Retrotestosterone (9/3,1 Oa-testosterone) has the hydrogen atom on carbon atom 9 in the jG-position and ring B has replaced the hydrogen normally found in the a-position. As we have seen, some substituted retrosteroids still possess androgenic and anabolic activity. [Pg.72]


See other pages where Hydrogen normalization is mentioned: [Pg.521]    [Pg.527]    [Pg.682]    [Pg.329]    [Pg.544]    [Pg.112]    [Pg.41]    [Pg.191]    [Pg.563]    [Pg.790]    [Pg.796]    [Pg.951]    [Pg.26]    [Pg.113]    [Pg.149]    [Pg.191]    [Pg.540]    [Pg.214]    [Pg.118]    [Pg.310]    [Pg.466]    [Pg.313]    [Pg.199]    [Pg.11]    [Pg.499]    [Pg.822]    [Pg.351]    [Pg.953]    [Pg.177]    [Pg.122]    [Pg.228]    [Pg.77]    [Pg.6]    [Pg.194]    [Pg.77]   
See also in sourсe #XX -- [ Pg.107 , Pg.108 , Pg.109 ]




SEARCH



Approximate Inversion-Curve Locus for Normal Hydrogen

Compressibility Factors for Normal Hydrogen

Hydrogen atom normal state

Hydrogen atom orbital normalization

Hydrogen bond normal

Hydrogen bonding normal

Hydrogen bonding normal phase

Hydrogen normal

Hydrogen normal

Hydrogen normalized current density

Hydrogenic radial function normalization

Normal Standard Hydrogen Electrode

Normal hydrogen electrode

Normal hydrogen electrode NHE

Normal hydrogen electrode electrochemical cells

Normal hydrogen electrode half-reactions

Normal hydrogen electrode reduction potentials

Normal hydrogen electrode, definition

Normal hydrogen electrode, potential

Normal hydrogen electrode, potential absolute

Normal hydrogen half cell

Normal hydrogen scale

Potential hydrogen, normal

Potential of the normal hydrogen electrode

The Normal Hydrogen Atom

The normal hydrogen bond

Thermodynamic Properties of Normal Hydrogen

© 2024 chempedia.info