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Methane variations

Over the past 220 000 years methane concentrations ranged between 350 and 750ppbv, compared to modem values in excess of 1700-1800 (Fig. 18-15). Over tens of millennia, methane variations appear to correspond to northern hemisphere insolation changes, correlate with Vostok paleotemperatures (Chappel-... [Pg.483]

Figure 8 Methane variations during the most reeent glaeial period as recorded in ice cores from Greenland (GRIP) and Antarctica (Byrd, Vostok) (Blunier et al, 1998 Stauffer et aL, 1998). The records were correlated by statistical matching of the variations shown (Blunier et al. (1999) reproduced by permission of Kluwer Academic/Plenum Publishers from Reconstructing Ocean History A Window into the Future, 1999, pp. 121-138 (figure 1)). Figure 8 Methane variations during the most reeent glaeial period as recorded in ice cores from Greenland (GRIP) and Antarctica (Byrd, Vostok) (Blunier et al, 1998 Stauffer et aL, 1998). The records were correlated by statistical matching of the variations shown (Blunier et al. (1999) reproduced by permission of Kluwer Academic/Plenum Publishers from Reconstructing Ocean History A Window into the Future, 1999, pp. 121-138 (figure 1)).
Methane data show that this gas in the surface water is in near equilibrium with that in the air. Methane variations do occur in bays, coastal, and anoxic areas, but under open ocean conditions methane concentrations rarely if ever undergo large fluctuations. Methane shows no correlation with chlorophyll a or with any of the otha hght hydrocarbons measured. [Pg.169]

Figure 4.9 shows a plot of Eq. (4.12). As the purge fraction a is increased, the flow rate of purge increases, but the concentration of methane in the purge and recycle decreases. This variation (along with reactor conversion) is an important degree of freedom in the optimization of reaction and separation systems, as we shall see later. [Pg.112]

Figure 4.9 Variation of vapor mole fraction of methane with purge fraction. Figure 4.9 Variation of vapor mole fraction of methane with purge fraction.
In a variation of this method, isolation of the ben2hydrol derivative is not required. The methane base undergoes oxidative condensation in the presence of acid with the same or a different arylamine direcdy to the dye. New fuchsine [3248-91 -7] Cl Basic Violet 2 (16), is prepared by condensation of two moles of o-toluidine with formaldehyde in nitrobenzene in the presence of iron salts to give the corresponding substituted diphenylmethane base. This base is also not isolated, but undergoes an oxidative condensation with another mole of o-toluidine to produce the dye. [Pg.272]

Another method of manufacturing SiC by the decomposition of a gas mixture containing silane, propane, and hydrogen, and hydrogen chloride has been described (80). With such a mixture, it was possible to work at a relatively lower (1200°C) temperature and it was claimed that compact, homogeneous P SiC crystals were obtained. In a variation of this gas-phase synthesis theme, SiC has been produced from the reaction of SiCl and methane (81). SiC precipitates from 1000 to 3000°C. [Pg.466]

An anaerobic digester is a no-recycle complete mix reactor. Thus, its performance is independent of organic loading but is controlled by hydraulic retention time (HRT). Based on kinetic theoiy and values of the pseudo constants for methane bac teria, a minimum HRT of 3 to 4 days is required. To provide a safety factor and compensate for load variation as indicated earlier, HRT is kept in the range 10 to 30 days. Thickening of feed sludge is used to reduce the tank volume required... [Pg.2228]

Century organic vapour analysers are factory calibrated to measure total organic vapours according to a standard (methane). Since different organic vapours interact with the flame ionization detector (FID) to varying extents, it is vital that the instrument user be aware of the magnitude of the variation in order to obtain the most accurate data. Each user must determine relative responses for the individual instrument. [Pg.333]

It is clear that human action can affect seven of eight of the major gi eenhouse forcings carbon dioxide, methane, nitrous oxide, ozone, CFCs, aerosols, and water vapor. As studies of solar variation have shown, it is also clear that human action is not the only factor involved in determining the impact of these forcings. There is still substantial uncertainty regarding the actual climate impact of the climate forcings. [Pg.243]

The main disadvantage of this technique is that it relies on very accurate temperature measurement, particularly near the top of the temperature profile, so that the position of the 5°F point can be established and the tangent accurately constructed. Also, the end of the bed is predicted only from kinetic considerations when, in fact, other factors may be more important. In practice, however, although this introduces some scatter into successive measurements—as does variation in the duty required of the methanator—the technique has proved very satisfactory. [Pg.91]

These tests were performed to establish the limits in flexibility and operability of a methanation scheme. The two demonstration plants have been operated in order to determine the optimum design parameters as well as the possible variation range which can be tolerated without an effect on catalyst life and SNG specification. Using a recycle methanation system, the requirements for the synthesis gas concerning H2/CO ratio, C02 content, and higher hydrocarbon content are not fixed to a small range only the content of poisons should be kept to a minimum. The catalyst has proved thermostability and resistance to high steam content with a resultant expected life of more than 16,000 hrs. [Pg.131]

This linear variation in catalytic activation energy with potential and work function is quite noteworthy and, as we will see in the next sections and in Chapters 5 and 6, is intimately linked to the corresponding linear variation of heats of chemisorption with potential and work function. More specifically we will see that the linear decrease in the activation energies of ethylene and methane oxidation is due to the concomitant linear decrease in the heat of chemisorption of oxygen with increasing catalyst potential and work function. [Pg.164]

Top typical saturation curve and variation of mean electron energy with applied field. Middle fraction of the electron swarm exceeding the specific energy at each field strength. Calculated assuming constant collision cross-section and Maxwell-Boltzman distribution. Bottom variation of products typical of involvement of ionic precursors (methane) and excited intermediates (ethane) with applied field strength... [Pg.254]

Two of the many products of ethylene radiolysis—methane and propane—show no or only negligible variation with field strength. Methane is produced by a molecular elimination process, as evidenced by the inability of oxygen or nitric oxide to quench its formation even when these additives are present in 65 mole % concentration (34). Propane is completely eliminated by trace amounts of the above scavengers, suggesting methyl and ethyl radicals as precursors ... [Pg.255]

Fig. 1-2 Chemical data from the Vostok ice core. The graph of 5D can be taken as a proxy for temperature changes, as described in Chapter 18. CO2 and CH4 are greenhouse gases and vary in the same direction as temperature. Non-seasalt sulfate and methane sulfonic acid are both sulfur species existing in the particle phase, and are positively correlated with each other, but negatively with T. Major variations for all of these variables seem to correlate either positively or negatively with each other, indicating a coupled system. <5D, non-seasalt sulfate, and methane sulfonic acid data kindly provided by Dr Eric Saltzman. CO2 data are from Bamola et al. (1987) and Jouzel et al. (1993). CH4 data are from Chappellaz et al. (1990) and Jouzel et al. (1993). (ppmv = parts per million by volume ppbv = parts per billion by volime)... Fig. 1-2 Chemical data from the Vostok ice core. The graph of 5D can be taken as a proxy for temperature changes, as described in Chapter 18. CO2 and CH4 are greenhouse gases and vary in the same direction as temperature. Non-seasalt sulfate and methane sulfonic acid are both sulfur species existing in the particle phase, and are positively correlated with each other, but negatively with T. Major variations for all of these variables seem to correlate either positively or negatively with each other, indicating a coupled system. <5D, non-seasalt sulfate, and methane sulfonic acid data kindly provided by Dr Eric Saltzman. CO2 data are from Bamola et al. (1987) and Jouzel et al. (1993). CH4 data are from Chappellaz et al. (1990) and Jouzel et al. (1993). (ppmv = parts per million by volume ppbv = parts per billion by volime)...
The interstitial air trapped during this process preserves a largely unaltered record of the composition of past atmospheres on time scales as short as decades and as long as several hundred thousand years. Such records have provided critical information about past variations in carbon dioxide (CO2), methane (CH4), nitrous oxide (N2O), carbon monoxide (CO), and the isotopic composition of some of these trace species. In addition, studies of the major elements of air nitrogen, oxygen, and argon, and their isotopic composition, have contributed... [Pg.469]

Brook, E. J., Sowers. T., and Orchardo, J. (1996). Rapid variations in atmospheric methane concentration during the past 110 000 years. Science 273, 1087-1091. [Pg.494]

Electron Nuclear Dynamics (48) departs from a variational form where the state vector is both explicitly and implicitly time-dependent. A coherent state formulation for electron and nuclear motion is given and the relevant parameters are determined as functions of time from the Euler equations that define the stationary point of the functional. Yngve and his group have currently implemented the method for a determinantal electronic wave function and products of wave packets for the nuclei in the limit of zero width, a "classical" limit. Results are coming forth protons on methane (49), diatoms in laser fields (50), protons on water (51), and charge transfer (52) between oxygen and protons. [Pg.13]

Figure 4.2.13 shows the variation of the flame speed with the maximum tangential velocity obtained with vortex ring combustion in the same mixture atmosphere [29]. The cylinder diameter was 100 mm and various lean, stoichiometric, and rich methane/ air and propane/air mixtures were examined. The diameter of the propagating flame was also determined and the ratio of the flame diameter to the core diameter was also plotted against the maximum tangential velocity. [Pg.52]

Variation of the normalized remaining percentage of CH4 fuel (c/Cj) after a run, measured by the gas chromatography, plotted over a very wide range of normalized turbulent intensities (u /Sl 10 100), where the subscript "i" refers to the initial condition. Both very rich (0 = 1.45 Cj = 13.2%) and very lean = 0.6 q = 5.92%) pure methane/air mixtures are investigated, showing critical values of Ka for the transition across which global quench occurs. [Pg.113]


See other pages where Methane variations is mentioned: [Pg.323]    [Pg.4328]    [Pg.178]    [Pg.323]    [Pg.4328]    [Pg.178]    [Pg.99]    [Pg.2]    [Pg.369]    [Pg.216]    [Pg.14]    [Pg.369]    [Pg.525]    [Pg.277]    [Pg.294]    [Pg.264]    [Pg.128]    [Pg.32]    [Pg.106]    [Pg.202]    [Pg.316]    [Pg.139]    [Pg.202]    [Pg.201]    [Pg.101]    [Pg.468]    [Pg.483]    [Pg.21]    [Pg.192]    [Pg.866]    [Pg.867]    [Pg.900]    [Pg.116]   
See also in sourсe #XX -- [ Pg.247 , Pg.248 , Pg.249 , Pg.259 ]




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