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Charge, additional

The unit has virtually the same flow sheet (see Fig. 2) as that of methanol carbonylation to acetic acid (qv). Any water present in the methyl acetate feed is destroyed by recycle anhydride. Water impairs the catalyst. Carbonylation occurs in a sparged reactor, fitted with baffles to diminish entrainment of the catalyst-rich Hquid. Carbon monoxide is introduced at about 15—18 MPa from centrifugal, multistage compressors. Gaseous dimethyl ether from the reactor is recycled with the CO and occasional injections of methyl iodide and methyl acetate may be introduced. Near the end of the life of a catalyst charge, additional rhodium chloride, with or without a ligand, can be put into the system to increase anhydride production based on net noble metal introduced. The reaction is exothermic, thus no heat need be added and surplus heat can be recovered as low pressure steam. [Pg.77]

However, reaction of 218 (E = P, R = R = H, R = r" = Me) with rerr-butyl-lithium most probably yields 221. The phospholyl loses its electrophilicity and the iron atom bears a considerable negative charge. Addition of rerr-butyllithium (one equivalent) followed by methyl iodide (one equivalent) does not give any isolable product but leads to recovery of the starting 218 only. In excess tert-butyllithium and methyliodide, 222 (R = r-Bu, R = Me) was isolated (81IC3252). [Pg.156]

The influence of inhibitor on the performance of a semi-continuous reactor can be, in some ways, similar to both batch and continuous systems. A dead time is usually observed upon addition of the initial charge. When the secondary stream flow is started after some reaction of the initial charge, additional inhibitor flows into the reactor and the initiation rate drops. When this programmed addition is stopped the initiation rate increases sometimes enough to cause temperature control problems. [Pg.4]

Gravity feed is to be used for charging additives to the reactor, for discharging the reactor to the hold tanks, and for feeding the dryer. [Pg.153]

Figure 22 Cyclic voltammograms recorded in aqueous solutions of Rieske fragments from (a) bci complex glassy carbon working electrode pH 7.2 (b) (recombinant) biphenyldioxygenase (basal) pyrolitic graphite working electrode (in the presence of the positively charged additive neomycin) pH 7.0. Scan rate 0.01 V s ... Figure 22 Cyclic voltammograms recorded in aqueous solutions of Rieske fragments from (a) bci complex glassy carbon working electrode pH 7.2 (b) (recombinant) biphenyldioxygenase (basal) pyrolitic graphite working electrode (in the presence of the positively charged additive neomycin) pH 7.0. Scan rate 0.01 V s ...
In confirmation of such an electrostatic interaction, the addition of positively charged additives compromises the response, Figure 32b.59... [Pg.568]

Hepatocytes are the dominant cell type in the Hver constituting approx. 70% of all hver cells. They are responsible for the uptake of substances from the blood and for the excretion by the bihary system. Specific requirements have to be met by compounds to be able to enter the hepatocytes. These are definite ranges of molecular weight, lipophiHcity and polarity or charge. Additionally, receptor-mediated transport systems of the hepatocytes pose further requirements on the structure of the substance. [Pg.184]

Semibatch, reactant A batch alkylation where a gaseous alkene is continuously charged addition... [Pg.388]

The complex is composed of a three-lattice layer of octahedral alumina and two tetrahedral silica sheets. The aluminum is substituted to varying degrees by magnesium (with sodium or potassium for balance of electrical charge). Additional elements present in small amounts include iron, lithium, titanium, calcium, and carbon. [Pg.418]

For nonionized compounds, or to change selectivity for ionized compounds, buffer additives such as micellar sodium dodecyl sulfate (SDS) or an octane/ butan-l-ol/SDS microemulsion may be used. For nonionic compounds, separation is based on distribution between the buffer and the charged additive, which moves at a different velocity than the background electrolyte. For charged species, separation is based on both the partitioning and the electrophoretic mobility of the sample components. Samples that are not soluble in aqueous media may be separated in organic solvents such as methanol or acetonitrile containing a conductive salt. ... [Pg.380]


See other pages where Charge, additional is mentioned: [Pg.397]    [Pg.1335]    [Pg.900]    [Pg.1263]    [Pg.153]    [Pg.287]    [Pg.12]    [Pg.13]    [Pg.557]    [Pg.564]    [Pg.565]    [Pg.566]    [Pg.568]    [Pg.867]    [Pg.92]    [Pg.186]    [Pg.565]    [Pg.140]    [Pg.277]    [Pg.43]    [Pg.271]    [Pg.15]    [Pg.86]    [Pg.87]    [Pg.1263]    [Pg.397]    [Pg.1158]    [Pg.83]    [Pg.601]    [Pg.2032]    [Pg.86]    [Pg.274]    [Pg.65]    [Pg.287]    [Pg.185]    [Pg.196]    [Pg.67]    [Pg.216]   
See also in sourсe #XX -- [ Pg.88 ]




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Addition charge-directed

Addition of Monodentate Charge-Neutral Nucleophiles

Additivity of Effective Charge in Reactants and Products

Additivity of effective charge

Additivity, inductive effects effective charge

Charge transfer, oxidative addition

Effective charge, additivity

Effective charge, additivity conservation

Effective charge, additivity equilibria

Effective charge, additivity rates

Spectra from Ionization by the Addition or Removal of Charges

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