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Substitutes for

The most reliable estimates of the parameters are obtained from multiple measurements, usually a series of vapor-liquid equilibrium data (T, P, x and y). Because the number of data points exceeds the number of parameters to be estimated, the equilibrium equations are not exactly satisfied for all experimental measurements. Exact agreement between the model and experiment is not achieved due to random and systematic errors in the data and due to inadequacies of the model. The optimum parameters should, therefore, be found by satisfaction of some selected statistical criterion, as discussed in Chapter 6. However, regardless of statistical sophistication, there is no substitute for reliable experimental data. [Pg.44]

The maximum-likelihood method, like any statistical tool, is useful for correlating and critically examining experimental information. However, it can never be a substitute for that information. While a statistical tool is useful for minimizing the required experimental effort, reliable calculated phase equilibria can only be obtained if at least some pertinent and reliable experimental data are at hand. [Pg.108]

Consider now thermal coupling of the prefractionator arrangement from Fig. 5.116. Figure 5.16a shows a prefi-actionator arrangement with partial condenser and reboiler on the prefractionator. Figure 5.166 shows the equivalent thermally coupled prefractionator arrangement sometimes known as a Petlyuk column. To make the two arrangements in Fig. 5.16 equivalent, the thermally coupled prefractionator requires extra plates to substitute for the prefractionator condenser and reboiler. [Pg.152]

Now recalculate the network area target substituting for in Fig. 7.5. Table 7.2 is revised to the values shown in Table 7.3 ... [Pg.231]

A mixture of polymethylene glycols of the type (CH20) ,xH20 where n is 6- 50. It is a white, amorphous powder having the odour of meth-anal, m.p. I20-130°C. The commercial product contains 95% methanal and is obtained in while flocculent masses when solutions of methanal are evaporated or allowed to stand. When heated it is converted to methanal. Used as a convenient solid substitute for methanal. [Pg.296]

In this instance a second aromatic ring can be substituted for two adjacent hydrogen atoms giving condensed polynuclear aromatics, for... [Pg.6]

Or by a naphthenic ring which can also be substituted for two adjacent hydrogen atoms forming a naphthene aromatic such as tetralin or tetra.hydronaphthaiLene. ... [Pg.7]

Other methods for analyzing combustion products can be substituted for chromatography. Gravimetry can be used, for example, after a series of absorption on different beds, as in the case of water absorption in magnesium perchlorate or CO2 in soda lime infra-red spectrometry can be used for the detection of CO2 and water. [Pg.29]

Hydrorefining can substitute for extraction processes such as furfural where it integrates perfectly into the conventional process scheme. [Pg.396]

The second tenu in the Omstein-Zemike equation is a convolution integral. Substituting for h r) in the integrand, followed by repeated iteration, shows that h(r) is the sum of convolutions of c-fiinctions or bonds containing one or more c-fiinctions in series. Representing this graphically with c(r) = o-o, we see that... [Pg.471]

Plenary 21B. A C Albrecht et al, e-mail address aca7 comell.edu (I CRS) (substituting for plenary 21 A). Discusses four new applications using a third approach to the Class II spectroscopies (see above). Raman... [Pg.1219]

Eleetron energy-loss speetroseopy is used for obtaining speetroseopie data as a eonvenient substitute for optieal speetroseopy, and, taking advantage of diflferenees in seleetion rules, as an adjimet to optieal speetroseopy. In addition, eleetron speetroseopy has many applieations to ehemieal and stnietural analysis of samples in the gas phase, in the solid phase, and at the solid-gas interfaee. [Pg.1322]

If the atom has nonzero nuclear spin /tlien F = S + I substitutes for S in equation (Cl.4.49), tire g-factor generalizes to... [Pg.2472]

Yet another form for the equations, this time expressed in terms of the can be obtained by substituting for N and the from equations (5.5) into (5.7) and (5,8). After a little rearrangement the result can be written... [Pg.36]

Substituting for the from equation (5,44) and simplifying then gives... [Pg.48]

We may substitute for p from this into equations (12.24) and (12.25) then, on passing to the limit - only terras of zeroth order in need be retained." Consequently the flux relations reduce to... [Pg.165]

We now introduce the atomic orbital expansion for the orbitals i/), and substitute for the corresponding spin orbital Xi into the Hartree-Fock equation,/,(l)x,(l) = X (1) ... [Pg.77]

When the Coulomb and exchange operators are expressed in terms of the basis functions and the orbital expansion is substituted for xu then their contributions to the Fock matrix element take the following form ... [Pg.78]


See other pages where Substitutes for is mentioned: [Pg.13]    [Pg.50]    [Pg.135]    [Pg.199]    [Pg.375]    [Pg.23]    [Pg.640]    [Pg.197]    [Pg.241]    [Pg.605]    [Pg.1367]    [Pg.1934]    [Pg.2880]    [Pg.7]    [Pg.714]    [Pg.100]    [Pg.105]    [Pg.357]    [Pg.46]    [Pg.116]    [Pg.146]    [Pg.152]    [Pg.162]    [Pg.166]    [Pg.112]    [Pg.132]    [Pg.153]    [Pg.264]    [Pg.328]    [Pg.639]    [Pg.4]    [Pg.124]   
See also in sourсe #XX -- [ Pg.206 , Pg.207 ]

See also in sourсe #XX -- [ Pg.6 , Pg.14 , Pg.137 , Pg.140 , Pg.143 , Pg.146 , Pg.152 , Pg.164 , Pg.201 ]




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A General Mechanism for Electrophilic Aromatic Substitution

Activation parameters for substitution

Addition-elimination mechanism for nucleophilic aromatic substitution

Alpha substitution reaction evidence for mechanism

Azine substitution —cont kinetics for bicyclic azines

Azine substitution —cont kinetics for monocyclic azines

Bimolecular displacement mechanism for nucleophilic aromatic substitution

Blood substitutes for

Bronsted equation, for substitution

Carbonic anhydrase cobalt-for-zinc ion substitution

Carboxypeptidase cobalt-for-zinc ion substitution

Characteristic groups for substitutive nomenclature

Chemical Kinetics Evidence for Nucleophilic Substitution Mechanisms

Cobalt-for-zinc ion substitution

Criteria for Nucleophilic Aromatic Substitution

Cross-sectional substitution sequences for the stacking of phases

Data for Nucleophilic Heteroaromatic Substitution

Designing ceramics for injectable bone graft substitutes

Diazanaphthalenes halo-, kinetics for substitution

Direct Substitution For Stability Limit

Dissociation mechanism for substitution

Electron Pushing for Electrophilic Aromatic Substitutions

Electron Pushing for Nucleophilic Aromatic Substitution

Electrophiles for the Electrophilic Aromatic Substitution

Electrophilic aromatic substitution, acylation procedures for

Energy diagram for electrophilic aromatic substitution

Finite difference substitutes for

Finite difference substitutes for derivatives

For electrophilic aromatic substitution

For electrophilic aromatic substitution reactions

For meta- and para-substituted

For nucleophilic substitution

General Mechanism for Nucleophilic Acyl Substitution

General Procedure for Substituting Hydrogens with Fluorine

General mechanisms for substitution at a solvated metal ion

Generalized mechanism for electrophilic aromatic substitution

Groups for Substitutive Nomenclature

Hammett p-o relationship, for substitution

Heterovalent Oxygen Substitution for Fluoride Ions

Hydrazoic acid, safe substitute for

Impact—Applications of Thermal Spray as a Substitute for Plating

Inorganic oxidant substitution for oxygen

Inventory Levels Accounting for the Impact of Part Substitution

Isoquinoline, activation halo-, kinetics for substitution

Isosteric Substitution as a Strategy for the Design of Safer Chemicals

K) for Addition of Substituted Propyl Radicals to (Meth)acrylate Esters

Kinetic data for substitution and

Kinetic data for substitution and elimination reactions

Kinetic parameters for substitution

Legal precedents for the Substitution Principle

Mandatory planning for substitution

Mechanism for Electrophilic Aromatic Substitution

Mechanisms for nucleophilic aliphatic substitution at glycosides

Metal-substituted Molecular Sieves as Catalysts for Allylic and Benzylic Oxidations

Modifications at C-5 and Substitution for the Ring Oxygen

Monothioacetals activation for substitution of sulfur

Nomenclature types for substituted

Nomenclature types for substituted systems

Nucleophilic aromatic substitution for

Nucleophilic aromatic substitution for hydrogen

Nucleophilic substitution—continued heteroaryne mechanism for

Nucleophilic substitution—continued mechanisms for aromatic compounds

Nucleophilic substitution—continued nomenclature for, 394 (footnote

Nucleophilic substitution—continued of pyridine N-oxides, kinetics for

Nucleophilicity sequence for substitution

Optimal Pattern for Substitution

Partial rate factors for hydrogen exchange in some substituted aromatic compounds

Paths for substitution

Possible Mechanisms for Nucleophilic Substitution

Possible Mechanisms for Substitution Reactions

Potential energy diagrams for electrophilic aromatic substitution

Potential energy diagrams for nucleophilic substitution

Pyridazine nucleophilic substitution, kinetics for

Quinazoline halo-, kinetics for substitution

Quinolines, activation halogeno-, kinetics for substitution

Quinoxaline halo-, kinetics for substitution

Rate constant for substitution reactions

Rate law, for nucleophilic substitution

Reaction Paths for Nucleophilic Substitution (SN2) Reactions

Real-Time Substitution Decisions Chemical Alternative Assessment for Pentabromodiphenyl Ether

Relative Rates for Addition of Substituted Propyl Radicals to AN andS

Retailers target BFRs for substitution

Ring closure of ortho-substituted /anilines, for heterocycles

Ring closure of ortho-substituted t-anilines, for

Ring closure of ortho-substituted t-anilines, for heterocycles

Ring closure of ortho-substituted tanilines, for heterocycles

Rules of thumb for substituting an H-atom by a group

SUBSTITUTING THERMAL SPRAYING FOR ELECTROPLATING

Scattering Theory for Substitutional Electromigration

Scope for Substitution

Solvents substituting for

Starter cultures as substitutes for bread additives

Starter cultures as substitutes for meat additives

Starters as substitutes for additives

Strategies for Aromatic Synthesis Order of Group Substitution

Structure-Reactivity Relationships for Substituted Benzenes

Substituted for Concentration Ratio

Substitutes for Fat

Substitutes for charcoal

Substituting Equivalents Known for the Same Purpose

Substitution for halogens

Substitution for halogens phosphonium fluondes

Substitution for halogens potassium fluonde

Substitution of Freshwater for Marine Data (and Vice Versa)

Substitution rate constants for

Substitution reactions direct displacement mechanism for

Substitution reactions ionization mechanism for

Substitutions for Arenes and Arene Exchange Reactions

Substitutions for Dienes and Trienes

Substitutions, for unavailable

Substrates for substitution reactions

Summary of Data for Methyl-substituted Compounds

The Edwards Equation for Nucleophilic Aliphatic Substitution

The General Mechanism for Electrophilic Aromatic Substitution Reactions

The Rate Law for Associative Substitutions

The case for other substitute drugs

Two Mechanisms for Nucleophilic Substitution

Used for Allylic Substitutions

Values for some substituted acetic acids

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