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System reduction

This cycle, as shown in Figure 2-23, is a regenerative cycle with water injection. Theoretically, it has the advantages of both the steam injection and regenerative systems reduction of NO emissions and higher efficiency. The work output of this system is about the same as that achieved in the steam injection cycle, but the thermal efficiency of the system is much higher. [Pg.81]

Just as selective oxidation can be carried out on these systems, reduction also occurs with considerable selectively. Hydrogenation of binaphthol (Pd catalyst) in glacial acetic acid at room temperature for seven days affords the octahydro (bis-tetrahydro) derivative in 92% yield with no apparent loss of optical activity when the reaction is conducted on optically pure material. The binaphthol may then be converted into the bis-binaphthyl crown in the usual fashion. [Pg.50]

Central nervous system Reduction of body weight Reduced appetite changed expression of anorexigenic (e.g., POMC) and orexigenic (e.g., NPY) hypothalamic neuropeptides... [Pg.634]

Sargeson and co-workers have reported the use of [Pt(en)3]4+ in template reactions to produce the platinum(IV) complexes of the macrobicyclic ligands sep and (N02)2sar (170).477 These reactions are analogous to those that occur around cobalt(III). However, in contrast to the [Co((N02)2sar)]3+ system, reduction of the pendant dinitro groups did not yield amines, but hydroxyamine groups.478... [Pg.729]

Reducing system Reduction potential (mV) at 50 °C (platinum electrode)... [Pg.423]

The transformation of the cyano group could also introduce a new chiral center under diastereoselective control (Figure 5.13). Grignard-transimination-reduction sequences have been employed in a synthesis of heterocyclic analogues of ephedrine [81]. The preferential formation of erythro-/3-amino alcohols may be explained by preferential hydride attack on the less-hindered face of the intermediate imine [82], and hydrocyanation of the imine would also appear to proceed via the same type of transition state. In the case of a,/3-unsaturated systems, reduction- transimination-reduction may be followed by protection of the /3-amino alcohol to an oxazolidinone, ozonolysis with oxidative workup, and alkali hydrolysis to give a-hydroxy-/3-amino acids [83]. This method has been successfully employed in the synthesis L-threo-sphingosine [84]. [Pg.117]

When less bulky ancillary ligands are used /3-hydride elimination leads to the formation of Q-olefins. As a consequence iminopyridine complexes are typically much less active than the diimine catalysts and afford lower-molecular-weight PE.321-324 For example, MAO/(122) polymerizes ethylene to branched oligomers with Mn < 600, and 240 branches per 1,000 carbons.325 Complex (123), is highly active for ethylene polymerization (820gmmol 1 h bar ).326 As with the diimine systems, reduction in the steric bulk of the ligand substituents results in reduced activity and lower-molecular-weight products. [Pg.17]

Hedeishi and McLaughlin [457] have reported the application of the Zeeman effect for the determination of mercury. Atomic absorption and atomic fluorescence techniques using closed system reduction-aeration have been applied widely to determine mercury concentrations in natural samples [458-472]. [Pg.197]

In a water/chlorobenzene biphasic system, reduction of aromatic aldehydes by hydrogen transfer from aqueous sodium formate catalyzed by [ RuCl2(TPPMS)2 2] provided unsaturated alcohols exclusively (Scheme 10.7). Addition of 3-CD shghtly inhibited the reaction [13]. It was speculated that this inhibition was probably due to complexation of the catalyst by inclusion of one of the non-sulfonated phenyl rings of the TPPMS ligand, however, no evidence was offered. [Pg.236]

Interposing an additional carbon atom between the indazole nucleus and the acetic acid side chain provides another compound that shows anti-inflammatory activity in model systems. Reduction of the carboxylic acid in the indazole (38-1) by means of hthium aluminum hydride leads to the carbinol (38-2). Alkylation of the enolate from the alcohol with methyl 2-bromo-2-methylpropionate leads to the corresponding ether. Saponification gives the free acid and thus bindarit (38-3) [40]. [Pg.408]

No separation Evaporation flow in the horizontal sense Flooding of paper from the electrodes Good dissipation of heat (thin wall and cooling system) reduction of heat (lower n, thinner paper) Regulation of electrode flow or cascade electrodes... [Pg.117]

In fused-salt systems, reduction of traces of water (if present) or of the metal cations ordinarily will be the cathodic limiting process. [Pg.209]

The aim of the project reported here is to develop system reduction methods for large biochemical systems, including silicon cell models. Here we present our first approach using balanced truncation. The plan is to develop reduction methods custom-made for biochemical systems. To use balanced truncation is a natural first step towards the development of finer methods, since it is a basic method in system theory, and many other methods are variants of this. [Pg.410]

This work is a first approach to system reduction for biochemical systems. The research perspective is to apply system reduction to a large biochemical system, possibly using decomposition of the system into small subsystems or modules. Moreover, system reduction methods have to be developed which apply to nonlinear systems with state variables that remain positive when starting with positive initial concentrations, and produce systems with the same properties, which admit a biological interpretation. [Pg.418]

Hardin, H. Van Schuppen,). H. System reduction of nonlinear positive systems by linearization and truncation. (Lecture notes in control and information sciences). Springer, Berlin/Heidelberg, 2006, pp 431-438. [Pg.424]

Satoh, T., Suzuki, S., Suzuki, Y., Miyaji, Y., and Imai, Z., Reduction of organic compound with sodium borohydride-transition metal salt systems reduction of organic nitrile, nitro and amide compounds to primary amines, Tetrahedron Lett., 10, 4555 4558, 1969. [Pg.93]


See other pages where System reduction is mentioned: [Pg.96]    [Pg.148]    [Pg.62]    [Pg.49]    [Pg.70]    [Pg.514]    [Pg.150]    [Pg.215]    [Pg.115]    [Pg.158]    [Pg.342]    [Pg.71]    [Pg.1066]    [Pg.251]    [Pg.770]    [Pg.29]    [Pg.21]    [Pg.686]    [Pg.29]    [Pg.160]    [Pg.169]    [Pg.117]    [Pg.686]    [Pg.44]    [Pg.95]    [Pg.103]    [Pg.820]    [Pg.71]    [Pg.332]    [Pg.103]    [Pg.96]   
See also in sourсe #XX -- [ Pg.418 ]




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Acyclic systems reduction

Alternative Reduction Systems

Automatic risk reduction systems

Biocatalytic reduction system

Biological systems oxidation reduction

Biological systems oxidation-reduction reactions

Bovine serum albumin +reductant systems

Catalytic system, toward reduction

Chromium reductant systems

Conjugated systems reduction

Conventional reduction-precipitation system

Corrosion redox system reduction

Cyclic Oxidation-Reduction Systems

Differential Equations the Basic Reduction to First Order Systems

Dimensionality, compartmentalized systems reduction

Dinitrogen reduction catalytic systems

Direct ozone reduction system

Discrimination of Ions Based on Diffusion Speed and Its Reduction in Field-Driven Systems

Drag reduction mixed systems

Drag reduction, turbulent systems

Drag reduction, turbulent systems characteristics

Drug delivery systems toxicity reduction

Electroenzymatic reduction system

Emulsion reduction-oxidation systems

Enamine system, reduction

Enantioselective alternative reduction system

Enantioselective reduction oxazaborolidine catalyst system

Error reduction, systems approach

Fuel Cell System Cost Reduction

Hemoglobin reduction systems

Hydrogen peroxide—reductant system

Ketone reductions, homogeneous systems

Liquid volume reduction system

Manganese +reductant systems

Model Studies of Reductive Elimination in the Rh System

Nitrate reduction system scheme

Other Systems Involving Size Reduction

Oxidation-Reduction Balances of the Earth System

Oxidation-Reduction Systems

Oxidation-reduction catalytic systems

Oxidation-reduction electrodes systems

Oxidation-reduction potential systems affecting

Oxidation-reduction potentials of pyridine nucleotide system

Photochromic systems reduction-oxidation

Reaction Systems Model Reduction

Reagent Systems leavage of Disulfides by Reduction

Redox system reduction

Redox system reduction current density

Redox system reduction hydrogen evolution

Redox system reduction mechanism

Redox system reduction oxygen

Redox system reduction polarization

Reductant systems, chromium toxicity

Reduction biomimetic systems

Reduction in Acyclic Systems

Reduction multiphasic systems

Reduction of Redox Systems

Reduction of a System on One Isolated Level Surface

Reduction of aromatic systems

Reduction system, catalytic

Reduction-activation systems

Reduction-precipitation system

Reductive carboxylation system

Row Reduction and Systems of Linear Equations

Safety instrumentation systems risk reduction

Semiconductor Systems for Reduction

Solvent systems, for biocatalytic reductions

Sound Reduction in Air-Handling Systems

Stoichiometric Reduction Systems

System for Predictive Error Analysis and Reduction (SPEAR)

System for predictive error analysis and reduction

System modeling and model reduction

Thermodynamics reduction-type systems

Three reduction system

Vanadium Compounds on Biological Systems Cellular Growth, Oxidation-Reduction Pathways, and Enzymes

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