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Exactness

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]

It cannot be said at this stage exactly how great an excess of decane would be required in order to make Fig. 4.7d feasible. This would have to be established experimentally, but the size of the excess does not change the basic structure. [Pg.104]

A refrigeration system is a heat pump in which heat is absorbed below ambient temperature. Thus the appropriate placement principle for heat pumps applies in exactly the same way as for refrigeration cycles. The appropriate placement for refrigeration cycles is that they also should be across the pinch. As with heat pumps, refrigeration cycles also can be appropriately placed across utility pinches. It is common for refrigeration cycles to be placed across a utility pinch caused by maximizing cooling water duty. [Pg.206]

In general, the final network design should be achieved in the minimum number of units to keep down the capital cost (although this is not the only consideration to keep down the capital cost). To minimize the number of imits in Eq. (7.1), L should be zero and C should be a maximum. Assuming L to be zero in the final design is a reasonable assumption. However, what should be assumed about C Consider the network in Fig. 7.16, which has two components. For there to be two components, the heat duties for streams A and B must exactly balance the duties for streams E and F. Also, the heat duties for streams C and D must exactly balance the duties for streams G and H. Such balemces are likely to be unusual and not easy to predict. The safest assumption for C thus appears to be that there will be one component only, i.e., C = 1. This leads to an important special case when the network has a single component and is loop-free. In this case, ... [Pg.215]

These expressions define Pn-2n for number of 1-2 shells in series in terms of R and Xp in each shell. The expressions can be used to define the number of 1-2 shells in series required to satisfy a specified value of Xp in each shell for a given R and Pjv 2n- Hence the relationship can be inverted to find the value of N which satisfies Xp exactly in each 1-2 shell in the series ... [Pg.434]

Boyle s law At constant temperature the volume of a given mass of gas is inversely proportional to the pressure. Although exact at low pressures, the law is not accurately obeyed at high pressures because of the finite size of molecules and the existence of intermolecular forces. See van der Waals equation. [Pg.66]

After the primary step in a photochemical reaction, the secondary processes may be quite complicated, e.g. when atoms and free radicals are fcrnied. Consequently the quantum yield, i.e. the number of molecules which are caused to react for a single quantum of light absorbed, is only exceptionally equal to exactly unity. E.g. the quantum yield of the decomposition of methyl iodide by u.v. light is only about 10" because some of the free radicals formed re-combine. The quantum yield of the reaction of H2 -f- CI2 is 10 to 10 (and the mixture may explode) because this is a chain reaction. [Pg.310]

Vegard s law In phases in which there is a range of composition of solid solution then the cell dimensions vary linearly with the molar proportions of the constituents. The (aw is rarely followed exactly. [Pg.418]

When it comes to the heaviest of petroieum fractions, modern analytical methods are not able to isolate and characterize the molecules completely. In the absence of something better, the analyst separates the heavy fractions into different categories, which leads merely to definitions that are workable but are no longer in terms of exact structure. [Pg.13]

All have molecular weights of 226 to the nearest integer (C = 12, H = 1, S = 32), but the exact molecular weights differ slightly. A resolution of 2500 is necessary to separate molecules 1, 2 and 3 but 75,000 is required to separate molecule 4 from molecule 3 which explains why high resolution mass spectrometers are sdiiglit. [Pg.49]

Adaptations of this method have been proposed in order to take into account the band displacement due either to substitution on the aromatic ring, or to chains of different lengths. The variations consist, instead of measuring the absorbance at maximum absorption, of an integration of the absorbance curve over a specified range (Oelert s method, 1971). More exact, this method is used less often mainly because the Brandes method is simpler... [Pg.61]

A panoply of methods whose results can be widely scattered are available to the process engineer not knowing the pitfalls attached to this activity, he would like to have a unique method or an exact guideline for applying these methods. [Pg.106]

The acentric factor can be determined as a function of temperature by finding the exact properties supplied by the DIPPR. [Pg.113]

The exact calculation of the index is given in the ASTM D 2270 standard. The kinematic viscosity at 40°C (f/) of an oil whose viscosity index (V7) is being calculated is compared with those of two reference oils for which the viscosity indices are 0 and 100 respectively, and which have at 100°C the same kinematic viscosity as that of the oil being examined )... [Pg.132]

The experimental conditions used to determine the CFPP do not exactly reflect those observed in vehicles the differences are due to the spaces in the filter mesh which are much larger in the laboratory filter, the back-pressure and the cooling rate. Also, research is continuing on procedures that are more representative of the actual behavior of diesel fuel in a vehicle and which correlate better with the temperature said to be operability , the threshold value for the Incident. In 1993, the CEN looked at two new methods, one called SFPP proposed by Exxon Chemicals (David et al., 1993), the other called AGELFI and recommended by Agip, Elf and Fina (Hamon et al., 1993). [Pg.215]

These are carbon monoxide, CO, unburned hydrocarbons (HC), and the nitrogen oxides, NO. In the U.S.A., a program called Auto/Oil (Burns et al., 1992), conducted by automotive manufacturers and petroleum companies, examined the effect of overall parameters of fuel composition on evaporative emissions and in the exhaust gases. The variables examined were the aromatics content between 20 and 45%, the olefins content between 5 and 20%, the MTBE content between 0 and 15% and finally the distillation end point between 138 and 182°C (more exactly, the 95% distilled point). [Pg.259]

The TBP (True Bolling Point) distillation gives an almost exact picture of a crude petroieum by measuring the boiling points of the components making up the crude whence its name. [Pg.331]

When the two components are mixed together (say in a mixture of 10% ethane, 90% n-heptane) the bubble point curve and the dew point curve no longer coincide, and a two-phase envelope appears. Within this two-phase region, a mixture of liquid and gas exist, with both components being present in each phase in proportions dictated by the exact temperature and pressure, i.e. the composition of the liquid and gas phases within the two-phase envelope are not constant. The mixture has its own critical point C g. [Pg.100]

An alternative and commonly used representation of the range of reserves is the proven, proven plus probable, and proven plus probable plus possible definition. The exact cumulative probability which these definitions correspond to on the expectation curve... [Pg.163]

A Monte Carlo simulation is fast to perform on a computer, and the presentation of the results is attractive. However, one cannot guarantee that the outcome of a Monte Carlo simulation run twice with the same input variables will yield exactly the same output, making the result less auditable. The more simulation runs performed, the less of a problem this becomes. The simulation as described does not indicate which of the input variables the result is most sensitive to, but one of the routines in Crystal Ball and Risk does allow a sensitivity analysis to be performed as the simulation is run.This is done by calculating the correlation coefficient of each input variable with the outcome (for example between area and UR). The higher the coefficient, the stronger the dependence between the input variable and the outcome. [Pg.167]

The exact relationship will depend upon both fluid and reservoir properties, and will be investigated during well planning. [Pg.220]

Schedule of Rates contract the cost of the labour is agreed on a rate basis, but the cost of materials and the exact hours are not specified. [Pg.301]

If you were offered 7,130 today, or 10,000 in exactly 5 years time, you should be indifferent to the options, unless you could find an alternative investment opportunity which yielded a guaranteed interest rate better than the bank (in which case you should accept the money today and take the alternative investment opportunity). [Pg.319]

The basic condition of the Standard application - the availability of stable coupled probabilistic or the multiple probabilistic relations between then controlled quality indexes and magnetic characteristics of steel. All the probabilistic estimates, used in the Standard, are applied at confidence level not less than 0,95. General requirements to the means of control and procedure of its performance are also stipulated. Engineers of standard development endeavoured take into consideration the existed practice of technical control performance and test at the enterprises that is why the preparation of object control for the performance of nondestructive test can be done during the process of ordinary acceptance test. It is suggested that every enterprise is operated in correspondence with direct and non-destructive tests, obtained exactly at it, for detailed process chart and definite product type, however the tests have long since been performed after development of the Standard displayed that process gives way to unification. [Pg.25]


See other pages where Exactness is mentioned: [Pg.84]    [Pg.97]    [Pg.103]    [Pg.413]    [Pg.14]    [Pg.161]    [Pg.206]    [Pg.214]    [Pg.235]    [Pg.240]    [Pg.328]    [Pg.371]    [Pg.49]    [Pg.54]    [Pg.56]    [Pg.62]    [Pg.179]    [Pg.198]    [Pg.198]    [Pg.218]    [Pg.102]    [Pg.184]    [Pg.12]    [Pg.16]    [Pg.30]    [Pg.59]   
See also in sourсe #XX -- [ Pg.39 , Pg.41 ]




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96 - exact values

An Exact Argument for a Hypothetical Solute

An Exact Gibbs Sampling Method

An exact MM approach to the theory of liquids

Analytical Characterization Exact Mass, Isotope Patterns, Charge State, Stoichiometry, Impurities

Application of an Exact Two-Structure Model (TSM)

Application of an exact two-structure model

Approximation exact

Approximations to Exact Perturbation and Response Theory Expressions

Asymptotic exact input/output linearization

Attempts at an Exact Theory

Augmented exact value

Boundary layers exact solutions

Bragg angle, deviation from exact

Buffered solutions exact treatment

Calculated exact mass

Calculations from experimental functions exact

Characteristics of the exact wave function

Charted Exact Solutions

Chase inverse exact

Collision source term exact

Comparison With Exact and Linearized Solutions

Comparison of Euler and backward Eulers methods with exact solution

Comparison of Eulers method with exact solution

Comparison with Exact Method

Comparison with Exact Results

Comparison with exact solutions

Comparisons numerically exact

Comparisons numerically exact results

Conduction exact

Conduction, heat exact solutions

Convergence toward exact solution

Copy-exactly approach

Correlation energy exact

Correlation potential, nonlocal, exact

Correlation wave function, exact

Corresponding states principle exact

Debating exact nature

Density functional theory exact exchange potential

Deriving Long Exact Sequences from Short Ones

Design space exact

Differentiability exact

Differentiability exact differential

Differentiability exact differential equation

Differential equations exact

Differential exact , tests

Differential, complete exact

Dirac equation exact solutions

EXACT controller

EXACT polymers

Electron correlations exact treatment

Energy exact atomic step

Euler’s test for exactness

Exact

Exact

Exact (non-adiabatic) theory

Exact 2-component

Exact 2-component Hamiltonian/method

Exact 2-component energies/results

Exact 2D structure search

Exact 2D substructure search

Exact Analytical Solution (Non-Steady-State Approximation)

Exact Analytical Solution (Steady-State Approximation)

Exact Arrhenius temperature dependence

Exact Bayesian Formulation and its Computational Difficulties

Exact Born-Oppenheimer molecular

Exact Born-Oppenheimer molecular orbitals

Exact Differentials and State Functions

Exact Discrete Formulation

Exact Expression for Cylindrical Channel EO Flow

Exact Foldy-Wouthuysen Transformation

Exact Formula for Front Velocity

Exact Formulation of the Adiabatic Theory

Exact Free Energy Calculations

Exact Gibbs sampling method

Exact Ground State of One- and Two-Dimensional Frustrated Quantum Spin Systems

Exact HF exchange

Exact Inversions from the Relaxation or Retardation Spectrum

Exact Kohn-Sham potentials

Exact MMCC theory

Exact Mass Measurements (High Resolution)

Exact Mass and Molecular Formulas

Exact Nuclidic Masses

Exact Relations Related to OPM

Exact Retarded Electromagnetic Interaction Energy

Exact Shape Factors

Exact Simulation of Sample Paths

Exact Solution for Chemical Reactions

Exact Solutions - Our Beacons

Exact Solutions for Cylindrical Bending

Exact Solutions of Linear Heat and Mass Transfer Equations

Exact Solutions of the Schroedinger Equation

Exact Solutions of the Stokes Equations

Exact Solutions to the Capillary Rise Problem

Exact Solutions. Critical conditions

Exact Theoretical Energies

Exact Thermodynamic Analysis

Exact Treatment of Buffered Solutions

Exact Treatment of Electron Correlations

Exact Two-Structure Model

Exact algorithms

Exact and Approximate Lumping

Exact and Approximate Wave Functions

Exact averages

Exact calculations

Exact cancellation condition

Exact cancellation methods

Exact conditions on the exchange-correlation hole

Exact confidence interval

Exact critical exponents for a polymer melt

Exact density of states and thermodynamics

Exact derivative

Exact diagonalization

Exact differential

Exact differential equations inexact

Exact differential equations of the first order

Exact differential expression

Exact differential properties

Exact differential, defined

Exact differentials definition

Exact differentials integration

Exact element method

Exact energy

Exact enumeration

Exact enumeration technique

Exact equation

Exact exchange

Exact exchange energy density functional

Exact exchange energy density functional from Fock operator

Exact exchange functionals

Exact exchange orbital functionals

Exact exchange potential

Exact exchange relations

Exact experimental methods. Surface-pressure measurements

Exact exponents in two dimensions

Exact fit

Exact formulation of centroid dynamics

Exact free energy, spinodal criterion

Exact function, Maxwell equation

Exact graft copolymer

Exact ground state

Exact hard-sphere scattering model

Exact image theory

Exact independent

Exact interest

Exact isotope masses

Exact kinetic approach

Exact kinetic energy

Exact linear-response theory

Exact local variant

Exact lumping

Exact mass

Exact mass data processing

Exact mass definition

Exact mass filtering

Exact mass measurement

Exact mass neutral loss

Exact mass table

Exact mass, exercise

Exact mass, notion

Exact match search

Exact mean field theory solution, plate macroions

Exact mean value equations

Exact measurements

Exact methods

Exact modal solutions

Exact models

Exact molecular weight

Exact nonreflective

Exact numbers

Exact numerical solution

Exact ordering search

Exact properties

Exact quantities

Exact quantum mechanical treatment

Exact resonance approximation

Exact restraint models

Exact results and theorems

Exact route

Exact sampling

Exact search strategy

Exact selection rules for electronic transitions

Exact sequence

Exact sequences, representations

Exact signal matching method

Exact solution for probabilities of complex particles

Exact solutions

Exact solutions for two-site exchange

Exact statistical analysis of designing sequences

Exact structure search

Exact threshold values

Exact trajectories

Exact transformation from paulions to bosons

Exact transformations

Exact treatment

Exact treatment of the Joule-Thomson coefficient

Exact two-component method

Exact wave functions

Exact wavefunction

Exact, but not quite correct, solutions

Exact-decoupling methods

Exact-exchange Methods

Exact-structure data

Exactive

Exactive

Exactly Solvable Cases

Exactly Solvable Models

Exactly Unitary Series Expansions

Exactly specified system

Exactness, test for

Exponent exact

First-order ordinary differential exact

Fisher Exact test

Fisher’s exact test

Form function of an isolated chain exact results

Formalism Using the Exact Hamiltonian

Fractals exact solution

Full configuration interaction exact solution of approximate problem

Hamiltonian exact

Hamiltonian exact 2-component

Hamiltonian exact Foldy-Wouthuysen-transformed

Heat transfer exact solutions

Inexact differential exact

Integral balance exact

Kinetic balance exact

LSD approximation exact locally

Leading Relativistic Corrections with Exact Mass Dependence

Line integral of an exact differential

Line integral of exact differential

Linear differential equation Exact

Linear differential forms, exact

Local Approximations to the Exact-Decoupling Transformation

Local exact decoupling

Long exact sequence of a pair

Mass differences, exact

Mass, exact determination

Mathematical interlude Exact and inexact differentials

Mathematical interlude. More properties of exact differentials The cyclic rule

Mayer-Vietoris long exact sequence

Measurement exact numbers

Metabolomics exact mass

Method exact enumeration

Molecular formulas of identical exact mass

Molecular orbitals exact relationships

Molecular system exact” wave function

Nonsmooth exact penalty function

Numbers Exact and Counted Versus Measured

Numerically exact solution

Operator exact expectation value

Oscillatory reactions some exact results

Partial exact searching

Particle-in-a-Box Exact Solution

Partition functions exact

Perturbation theory exact

Protein folding simple, exact models

Q Exactive

Quantum exact method

Random walks exact solution

Recent Progress in Understanding Exact Conditions

Relative Homology and the Associated Long Exact Sequence

Repeats, exact

Results for the exact exchange

SA type algorithms and convergence to the exact extreme

Schroedinger equation exact solutions

Short exact sequence

Significant figures exact numbers

Simple exact models

Size-extensivity of exact wave functions

Some Exact Conditions Satisfied by all Electronic Systems

Stokes equations exact solutions

Superposition approximation theories, exact solutions

Symmetry reduction exact solutions

Temperature exact differential

The Exact Mean Field Theory Solution for Plate Macroions

The Exact Muffin-Tin Orbital Method

The Exact Wavefunction

The FIND, SEARCH, REPLACE, SUBSTITUTE and EXACT Functions

The PDT and Thermodynamic Integration for Exact Quantum Free Energy Changes

The asymptotically exact equations

The exact electronic Schrodinger equation

The exact-counting method (partially attractive chains)

The localization exact sequence

Thermal force exact results

Time-Dependent Friction Function Exact Expression

Time-dependent density functional theory exact exchange

Tricritical swelling exponent in two dimensions estimations and exact values

Uniform density limit exact constraints

Valence Bond Formalism Using the Exact Hamiltonian

Viscoelastic functions exact

Wave functions exact, expansion

Waveguides with exact solutions

What Exactly Does Aloe Cure

Yang-Mills gauge field theory exact solutions

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