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Volatility update

Using Volatile Anaesthetic Agents. Dr. P. Fenton, Update in Anaesthesia, Practical Procedures, Issue 5,1995, http //www.nda.ox.ac.uk/wfsa/html/u05/u05 007.htm... [Pg.82]

Shah JJ, Heyerdahl EK. 1988. National ambient volatile organic compounds (VOCs) data base update. Research Triangle Park, NC U.S. Environmental Protection Agency, Office of Research and Development. [Pg.159]

The mechanisms for the NMHCs (except DMS) required to fully characterise OH chemistry were extracted from a recently updated version of the Master Chemical Mechanism (MCM 3.0, available at http //mcm.leeds.ac.uk/MCM/). The MCM treats the degradation of 125 volatile organic compounds (VOCs) and considers oxidation by OH, NO3, and O3, as well as the chemistry of the subsequent oxidation products. These steps continue until CO2 and H2O are formed as final products of the oxidation. The MCM has been constructed using chemical kinetics data (rate coefficients, branching ratios, reaction products, absorption cross sections and quantum yields) taken from several recent evaluations and reviews or estimated according to the MCM protocol (Jenkin et al., 1997, 2003 Saunders et al., 2003). The MCM is an explicit mechanism and, as such, does not suffer from the limitations of a lumped scheme or one containing surrogate species to represent the chemistry of many species. [Pg.4]

EPA. 1994i. Method 0030. Volatile organic sampling train. Method Status Table SW-846, third edition updates I, II, IIA and IIB. U. S. Environmental Protection Agency. [Pg.234]

Two methods, EPA SW-846 8015 and 8015A, were, in the past, often quoted as the source of gas chromatography-based methods for measurement of the total petroleum hydrocarbons in a sample. However, the original methods were developed for nonhalogenated volatile organic compounds and were designed to measure a short target list of chemical solvents rather than petroleum hydrocarbons. Thus, because there was no universal method for total petroleum hydrocarbons, there were many variations of these methods. Recently, an updated method... [Pg.192]

Garner, K. and S. Smith. Volatile Organic Compounds, the good, the bad and the analysis, SPME, University of the West of England, Bristol updated 9/23/04 visited 9/19/05 http //www.chemsoc.org/exemplarchem/entries/2004/westengland smith/Ex-emp Web/methdev. htm. [Pg.33]

Sauer, T.C., Jr, Sackett, W.M. Jeffrey, L.M. (1978) Volatile liquid hydrocarbotrs in the surface coastal waters of the Gulf of Mexico. Marine Chem., 1, 1-16 Seifert, B. Abraham, H.-J. (1982) Indoor air concentratiotrs of benzene and some other aromatic hydrocarbons. Ecotoxicol. environ. Saf, 6, 190-192 Shah, J.J. Heyerdahl, E.K. (1988) National Ambient Volatile Organic Compounds (VOCs) Data Base Update (EPA 600/3-88/0 lOA), Research Triangle Park, NC, Environmental Protection Agency, Atmospheric Sciences Research Laboratory ... [Pg.264]

Column selection is not yet a precise science. There are no uniform theories for the separation mechanisms that operate for the resolution of enantiomers using the wide array of chiral stationary phases that are currently available. It is therefore strongly recommended that the literature is searched to determine whether the analyte under investigation has been separated and which chiral stationary phase was used. Many chiral food volatiles have now been separated and a comprehensive database has been compiled that is continually updated and contains most reported separations (Koppenhoefer et al., 1993 Roussel and Piras, 1993). There are many other sources in the literature (Anonymous, 1993a,b Konig, 1993 Maas et al., 1994 Schreier et al., 1995 Juchelka et al., 1998 Miranda et al., 1998). [Pg.1040]

AgBB/DIBt (2001) (last updated 2008) Health-related evaluation procedure for volatile organic compound emissions from... [Pg.144]

The first representative reference values for indoor air in German households were derived from a study conducted by the old Federal Health Office into around 500 households in West Germany in 1985/86 (Krause, Chutsch and Henke, 1991). In 2007 updated reference values for individual volatile organic compounds (VOCs) and for aldehydes (Tables 9.3 and 9.4) were derived from long-term sampling in >550 households by means of diffusion samplers. Additionally a number of mostly regional studies have been made in schools (Heinzow et al., 1994), day-care centers (Schreiner, Wetzel and Kirchbach, 2001) and offices (Schlechter et al., 2004). [Pg.204]

The Finite Difference Approximations and the Iterative Technique. The reaction kinetics are dependent on the rest of the equations through particle temperatures. If we have an initial guess on the coal particle temperature history during its total residence in the reactor then the relations given by Eq. (15) are decoupled from the rest and can be solved separately. Consequently, the volatilization estimates, v j(t) s, can be used to update particle temperatures with Eqs. (11) through (14). [Pg.223]

The Kb method. For updating the tray temperatures, the theta method relies on the Kb method. The Kb method takes advantage of the near-linear dependence of the logarithm of the K-values and the relative volatilities on temperature over short temperature spans. Relative volatilities (a s) are calculated with respect to a base component K-value, K.bj k, at the stage temperature of the current column trial, Tjk. The base component is usually a middle boiler or a hypothetical component, The K-value of the base component for the next trial, Kbjk + 1( is calculated using a form of the bubble-point equation unique to the Kb method ... [Pg.154]

Update the outside-loop variables the reference base value, Khj Ref the relative volatilities, a,-, and parameters Aj and Bj of the K- value model, parameters a(j and 6 of the activity coefficient model and parameters Cjt DJt EJt and Fj of the enthalpy models, using the complex K-value and enthalpy correlations and the current set of temperatures and compositions. [Pg.176]

The outside-loop variables the relative volatilities, ct s the constants of the Kb model, A- s and B, s and the constants of the enthalpy models, Cj and Dj and Ej and Fj are not updated except in the outer loop. The factors, Sbj% R s, and RvJb, are initialized at the start of each inside loop. The base stripping factors enter in inside-loop solution where they are needed to get the stripping factors of the component material balances ... [Pg.178]

Shah, J. J., and Heyerdahl, E. K. National Ambient Volatile Organic Compounds (VOC) Data Base Update, U.S. Environmental Protection Agency, Washington, DC, 1988. [Pg.400]

Updated solar photospheric abundances are compared with meteoritic abundances. It is shown that only one group of chondritic meteorites, the Cl chondrites, matches solar abundances in refractory lithophile, siderophile, and volatile elements. All other chondritic meteorites differ from Cl chondrites. The agreement between solar and Cl abundances for all elements heavier than oxygen and excluding rare gases has constantly improved since Goldschmidt (1938) published his first comprehensive table of cosmic abundances. [Pg.62]

An updated design comprises recirculation of a pre-cooled hydrocarbon liquid with an mono-pump. The quench medium is immiscible with pyrolysis liquids due to the low polarity compared to pyrolysis liquids and can therefore be separated in the lower part of the quenching column and passed into the reservoir (7). Resisting aerosols are collected by electrostatic precipitators. Additionally, a cooler was installed to remove the fluidising gas from traces of lower volatile compounds (water etc.) (11). [Pg.1377]

The expectations of market players and eventual outcomes in relation to micro level allocation plans for the second phase will have considerable impact on the functioning of the market for CO2 allowances and therefore the success or failure of the scheme. The updating of allocation plans required by the Directive takes away an underlying assumption of most economic assessments of emission trading schemes, i.e. that distribution does not affect efficiency unless transaction costs are high. Updated allocation plans have the effect of altering the abatement and production choices made by participants. Where participants believe that the base years in future allocation plans will be updated there is an incentive to increase emissions. The uncertainty as to whether or not this will happen in the second NAPs is likely to result in increased volatility and illiquidity (wider bid-offer spreads)... [Pg.180]


See other pages where Volatility update is mentioned: [Pg.250]    [Pg.250]    [Pg.1626]    [Pg.209]    [Pg.34]    [Pg.208]    [Pg.528]    [Pg.285]    [Pg.307]    [Pg.250]    [Pg.1694]    [Pg.1626]    [Pg.223]    [Pg.316]    [Pg.181]    [Pg.742]    [Pg.846]    [Pg.410]    [Pg.91]    [Pg.234]    [Pg.1113]    [Pg.1626]   
See also in sourсe #XX -- [ Pg.793 ]




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