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Direct conversion

Upon low conversion direct photolysis the cis isomer (10) gave only the cis isomer (12) and the trans isomer (11) gave only the trans isomer (13). The triplet sensitized reaction of (10) and (11) gave rise only to cis-trans isomerization. Thus the di-ir-methane photorearrangement from the triplet state cannot compete with triplet state deactivation via cis-trans isomerization (Zimmerman has termed this the free rotor effect). Several other examples of regio-specilicity and stereospecificity in di-w-methane photoreactions are as followsa8 a3) ... [Pg.477]

As mentioned above, iridium complexes are also active in the formation of amines via the hydrosilylation/protodesUylation of imines. In the presence of 2 equiv. of HSiEts, the cationic complex [lr bis(pyrazol-l-yl)methane (CO)2][BPh4] (C4) catalyzes the reduction of various imines, including N-alkyl and N-aryl imines and both aldimines and ketimmes. Excellent conversions directly to the amine products were achieved rapidly at room temperature in a methanol solution (Scheme 14.7) [53]. [Pg.355]

An analogous implementation for the standard Ewald method has been presented [44]. Conversely, direct use of the Ewald sum [45] or approximations to it [46 18], which are pairwise decomposable and hence suitable for MC simulations, have generally proven to be too inefficient for most modern applications [49]. Additionally, it should be pointed out that Ewald sums — independent of implementation — are incompatible with implicit solvent models that model a spatially varying dielectric with anything more than trivial functional dependencies [45]. [Pg.58]

Influence of the downstream plants. Up to now, we have regarded the coal gasification reactor with the waste heat recovery system as an isolated unit. In the event that the gas generated is intended to be used as fuel gas, for example in a combined power station, this approach is justified. If, however, the gas is to be used as synthesis gas, the effect of the downstream units must be taken into consideration. In such cases it is necessary to feed the gas to a CO shift conversion unit in order to obtain the C0/H2 ratio required for the synthesis process. Apart from gasification at atmospheric pressure, which requires an intermediate compression step, it has proved advisable to locate the CO shift conversion directly downstream of the gasification section. A stage in which dust particles are removed from the gas is situated between these two units. It is assumed that exergy losses do not occur in this unit. [Pg.156]

Sakai, K., Nakamura, K., Wakayama, M., and Moriguchi, M. (1997). Change in nitrite conversion direction from oxidation to reduction in heterotrohpic bacteria depending on the aeration conditions. Joiimd/ of Fermentation and Bioengineering 84, 47—52. [Pg.257]

Of all the methods described, the most convenient laboratory preparation of NCAs is the reaction of Boc-protected amino acids with thionyl chloride in THF. The method provides NCAs in good yields, which may then be purified by crystallization. Typically, a urethane-protected amino acid in THF is treated with 1.1-4 equivalents of thionyl chloride at 0°C. The NCA is formed in 30 minutes to 24 hours, depending on the annino acid and the urethane protecting group. Conversely, direct phosgenation of an amino acid is the preferred industrial process and modifications, such as trimethylsilylation, allow preparation of NCAs... [Pg.505]

Surface chemistry, in general, is an area in which the ability to selectively modify the chemical and physical properties of an interface is highly desirable. The synthetic chemistry of surfaces is now in a developing stage, particularly with respect to the attachment of electroactive redox sites to metal or semiconductor surfaces (L-3). Single component and bilayer (4) electroactive films have been a field of intense research activity since their applications are apparent in catalysis, solar energy conversion, directed charge transfer, electrochromic devices, and trace analysis. [Pg.159]

The rotary kiln pyrolysis unit used in these experiments was originally used for studies in peat conversion directed by E. Chornet at the University of Sherbrooke, Quebec (Campion, 1978). [Pg.326]

If not the enzyme, one of its products might exert the regulatory function on DNA replication. The only deoxyribonucleotide without negative feedback action on ribonucleotide reductase, dCTP, has been advanced by Reichard to be involved. Addition of thymidine to hamster cells lowers the dCTP pool and concomitantly inhibits DNA synthesis even when dCTP has not become limiting as substrate . Under these conditions no more initiation of replication takes place and a specific correlation of the two results has been claimed. Conversely, direct inhibition of DNA synthesis by aphidico-... [Pg.81]

Ruben hadn t conversed directly with the original habitat for over forty years, not since his last visit. It was a trip which most Edenists made at some time in their life. Not a pilgrimage (they would hotly deny that) but paying their respects, acknowledging the sentimental debt to the founding entity of their culture. [Pg.135]

Dangerous fluctuation may occur in the PO IV conversion direction Use IV PO only. [Pg.254]

Some systems use the output fi om the lexical lookup process and/or grapheme-to-phoneme conversion directly as the input to the synthesizer. In some systems however, an additional step often known as post-lexical processing is performed which modifies the output in some way. The most significant factor in determining how much post lexical processing is the specific form of... [Pg.224]

Some systems use the output from the lexical lookup process and/or G2P conversion directly as the input to the synthesizer. In some systems, however, an additional step often known as post-lexical processing is performed, which modifies the output in some way. The most significant factor in determining how much post-lexical processing is performed is the specific form of the input to the synthesizer. This was discussed in Section 8.1.3, where we saw that we could choose high-level phonemic representation or a low-level detailed phonetic representation. A low-level representation will require significant processing, for example to turn an /n/ into an /m/ in a labial context, but, because... [Pg.223]


See other pages where Direct conversion is mentioned: [Pg.150]    [Pg.22]    [Pg.561]    [Pg.501]    [Pg.202]    [Pg.107]    [Pg.22]    [Pg.150]    [Pg.6]    [Pg.490]    [Pg.199]    [Pg.205]    [Pg.359]    [Pg.69]    [Pg.140]    [Pg.633]    [Pg.89]    [Pg.1177]    [Pg.490]    [Pg.1296]    [Pg.249]    [Pg.6635]    [Pg.291]    [Pg.538]    [Pg.115]    [Pg.118]    [Pg.92]    [Pg.115]    [Pg.115]    [Pg.185]    [Pg.538]    [Pg.60]    [Pg.574]    [Pg.709]   
See also in sourсe #XX -- [ Pg.23 , Pg.34 ]

See also in sourсe #XX -- [ Pg.50 ]




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Anode catalyst Direct conversion

Cathode catalyst Direct conversion

Cathodes Direct conversion

Cell components Direct conversion

Conversion tables direct equivalents

Direct Conversion of Nitroalkenes to Carbonyl Compounds

Direct conversion of coal

Direct conversion to disulphide

Direct energy conversion efficiency

Direct methane conversion

Direct microbial conversion

Direct microbial conversion lignocellulosic biomass

Direct or indirect conversion

Directive conversations

Directive conversations

Efficiencies Direct conversion

Electronic conductivity Direct conversion

Energy conversion membranes direct methanol fuel cells

Fuel cell technology Direct conversion

Half-cell Direct conversion

Hydrogen sulfide direct conversion

Molten carbonate Direct conversion

Ohmic Direct conversion

Overall efficiency Direct conversion

Solid oxide fuel cell Direct conversion

Supportive conversations flow direction

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