Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Water-methanal

Several alternative methods have been considered in order to increase the energy density of natural gas and facilitate its use as a road vehicle fuel. It can be dissolved in organic solvents, contained in a molecular cage (clathrate), and it may be adsorbed in a porous medium. The use of solvents has been tested experimentally but there has been little improvement so far over the methane density obtained by simple compression. Clathrates of methane and water, (methane hydrates) have been widely investigated but seem to offer little advantage over ANG [4]. Theoretical comparison of these storage techniques has been made by Dignam [5]. In practical terms, ANG has shown the most promise so far of these three alternatives to CNG and LNG. [Pg.274]

Barrer s discussion4 of his analog of Eq. 28 merits some comment. Equation 28 expresses the equilibrium condition between ice and hydrate. As such it is valid for all equilibria in which the two phases coexist and not only for univariant equilibria corresponding with a P—7" line in the phase diagram. (It holds, for instance, in the entire ice-hydratell-gas region of the ternary system water-methane-propane considered in Section III.C.(2).) In addition to Eq. 28 one has Clapeyron s equation... [Pg.23]

A nonlinear molecule, such as water, methane, or benzene, can rotate about any of three perpendicular axes, and so it has three rotational modes of motion. The average rotational energy of such a molecule is therefore 3 X jkT = ]kT. The contribution of rotation to the molar internal energy of a gas of nonlinear molecules is therefore... [Pg.351]

Frequently we are dealing with the special but common situation that the system has an even number of electrons which are all paired to give an overall singlet, so-called closed-shell systems. The vast majority of all normal compounds, such as water, methane or most other ground state species in organic or inorganic chemistry, belongs to this class. In these... [Pg.30]

Polyesters, such as microbially produced poly[(P)-3-hydroxybutyric acid] [poly(3HB)], other poly[(P)-hydroxyalkanoic acids] [poly(HA)] and related biosynthetic or chemosynthetic polyesters are a class of polymers that have potential applications as thermoplastic elastomers. In contrast to poly(ethylene) and similar polymers with saturated, non-functionalized carbon backbones, poly(HA) can be biodegraded to water, methane, and/or carbon dioxide. This review provides an overview of the microbiology, biochemistry and molecular biology of poly(HA) biodegradation. In particular, the properties of extracellular and intracellular poly(HA) hydrolyzing enzymes [poly(HA) depolymerases] are described. [Pg.289]

Fig. 2.5.11. (a) APCI-LC-MS(+), (b) ESI-LC-MS(-t-), (c) ESI-LC-MS(+), (d) ESI-LC-MS(+), (e) APCI-LC-MS(—) and (f) ESI-LC-MS(—) reconstructed ion chromatograms (RIC) of methanolic solution of the household detergent mixture as in Fig. 2.5.2. Chromatographic conditions (a), (b), (e), and (f) RP-Cig, methanol/water gradient elution (c) ion-pairing RP-Cla using trifluoro acetic acid (TFA) (5 mmol), methanol/water gradient elution (d) isocratic elution performed on PLRP-column, eluent methanol/water methane... Fig. 2.5.11. (a) APCI-LC-MS(+), (b) ESI-LC-MS(-t-), (c) ESI-LC-MS(+), (d) ESI-LC-MS(+), (e) APCI-LC-MS(—) and (f) ESI-LC-MS(—) reconstructed ion chromatograms (RIC) of methanolic solution of the household detergent mixture as in Fig. 2.5.2. Chromatographic conditions (a), (b), (e), and (f) RP-Cig, methanol/water gradient elution (c) ion-pairing RP-Cla using trifluoro acetic acid (TFA) (5 mmol), methanol/water gradient elution (d) isocratic elution performed on PLRP-column, eluent methanol/water methane...
The aim of the present work was to design and operate an apparatus in which stationary combustion and flames can be produced and sustained to pressures of 2000 bar and with environmental temperatures up to 500°C. Visual observation of the interior of the reaction vessel should be possible. Arrangements had to be made by which a gas flow of only a few microlitres per second could be fed steadily into the reaction vessel at pressures to two kilobar. A similar provision was necessary to extract small samples for product analysis at constant conditions. The principle of design and operation will be described. First results will be given for experiments with oxygen introduced into supercritical water-methane mixtures. [Pg.2]

Although the concentric nozzle (see Fig. 1 b) and the twin set of feed autoclaves permitted the simultaneous introduction of two gases into the reaction cell, during the present experiments only one gas was introduced at a time. In most cases this was oxygen into a supercritical water-methane mixture. The oxygen flow was adjusted to constant values between 1 and 6 mm s , determined from the bellows... [Pg.3]

Within the frame of the present first series of experiments it was almost always oxygen which was injected into supercritical water-methane mixtures. There were several reasons for this first choice. One of these was the desire, to study rich flames and their possible products first. Often the water to methane mole fraction ratio was 0.7 to 0.3. But mixtures down to a methane mole fraction of 0.1 were also used. It was possible, however, to inject oxygen and methane simultaneously into the supercritical water and produce a flame. Not possible was the production of true premixed flames. After a retraction of the thin inner nozzle capillary of the burner (see Fig. 1 b) the two gases could be mixed just below the reaction cell, but the flame reaction proceeded from the nozzle tip in the cell back towards this mixing point immediately. [Pg.3]

The figures 2 to 5 show photographs of typical flames produced by oxygen injection into water-methane phases at 450°C and pressures of 300, 600, 1000 and 2000 bar. The flow velocity as given by the oxygen feed autoclave s bellows compression at these pressures and room temperature was about 3 mm s for the first three pressures and about... [Pg.3]

Yamaki, D., Koch, H., Ten-no, S. Basis set limits of the second order Moller-Plesset correlation energies of water, methane, acetylene, ethylene, and benzene. J. Chem. Phys. 2007, 127, 144104. [Pg.147]

Kabashima H, Einaga H, Futamura S (2003) Hydrogen evolution from water, methane and methanol with nonthermal plasma. IEEE Transactions on Industry Applications 39 340-345... [Pg.111]

Diagram on the left shows the composition of the solar nebula (abundances in wt. %). Diagram on the right expands metals (astronomical jargon) into ices (water, methane, and ammonia) and rock (all other remaining elements). Jupiter and Saturn formed mostly from nebular gases, Uranus and Neptune formed mostly from ices, and the terrestrial planets formed primarily from rock. [Pg.508]

High Temperature Reaction. Reaction in the high temperature regime produces carbon monoxide, water, methane, formaldehyde, and methanol (8) the two higher ketones also form ethylene (I). The intermediate responsible for chain branching appears to be formaldehyde. The concentration of formaldehyde and the rate of reaction run parallel over the whole of the reaction, as shown in Figure 4 for diethyl ketone. [Pg.105]

Effect of other factors on cellulose. Dry distillation at a temperature above 150°C causes cellulose to produce compounds of low molecular weight, such as water, methane, ethylene, carbon monoxide, carbon dioxide, acetic acid, and acetone. According to Pictet [49] dry distillation under reduced pressure yields a substance having the empirical formula C6H10Oj, laevo-glucosan which probably is /3-D-glucopyranose anhydride ... [Pg.227]

Figure 7.1-3. Steady flame when oxygen is injected into supercritical 70/30 water/methane mixture at 100 MPa and 450°C. Figure 7.1-3. Steady flame when oxygen is injected into supercritical 70/30 water/methane mixture at 100 MPa and 450°C.
Pressure reductions have been observed for methane hydrate formation when organic components (that are very insoluble in water) are added to the water + methane system. These organic components include THP, cyclobutanone, methylcyclohexane, CHF3, and CF4 (Mooijer-van den Heuvel et al., 2000 ... [Pg.81]

Molecular dynamics (MD) simulation studies also indicate that the initial formation of methane hydrate occurs preferentially near the water-methane interface where there is a significant concentration gradient (Moon et al., 2003). [Pg.130]

Figure 3.27 Methane hydrate film development at the water-methane interface from dissolved methane in the aqueous phase, as indicated from Raman spectroscopy (a) and methane solubility predictions (b). (a) A series of Raman spectra of dissolved methane collected at different temperatures during the continuous cooling process. Spectra marked A through E correspond to temperatures of 24°C, 20°C, 15.6°C, 10.2°C, and 2.8°C, respectively. (b) A schematic illustration of temperature dependencies of the equilibrium methane concentration in liquid water (C = without hydrate, Qjh = with hydrate). The scale of the vertical axis is arbitrary, but the Raman peak area is proportional to methane dissolved in water. Points A through F correspond to different temperatures during the continuous cooling process. (From Subramanian, S., Measurements ofClathrate Hydrates Containing Methane and Ethane Using Raman Spectroscopy, Ph.D. Thesis, Colorado School of Mines, Golden, CO (2000). With permission.)... Figure 3.27 Methane hydrate film development at the water-methane interface from dissolved methane in the aqueous phase, as indicated from Raman spectroscopy (a) and methane solubility predictions (b). (a) A series of Raman spectra of dissolved methane collected at different temperatures during the continuous cooling process. Spectra marked A through E correspond to temperatures of 24°C, 20°C, 15.6°C, 10.2°C, and 2.8°C, respectively. (b) A schematic illustration of temperature dependencies of the equilibrium methane concentration in liquid water (C = without hydrate, Qjh = with hydrate). The scale of the vertical axis is arbitrary, but the Raman peak area is proportional to methane dissolved in water. Points A through F correspond to different temperatures during the continuous cooling process. (From Subramanian, S., Measurements ofClathrate Hydrates Containing Methane and Ethane Using Raman Spectroscopy, Ph.D. Thesis, Colorado School of Mines, Golden, CO (2000). With permission.)...
Stewart and Hack (5.) have presented operating characteristics of pressure swing adsorption systems for reducing impurities in a hydrogen stream from 40 vol percent to 1 ppm. Impurities included ammonia, water, methane, carbon monoxide, carbon dioxide, nitrogen, and several hydrocarbons. In this study heatless adsorption is used to separate hydrogen sulfide-hydrogen mixtures and the experimental results are compared with theoretical models. [Pg.261]

The benefit obtained from counter-flow depends on the particular separation, but it can often be substantial, particularly in gas separation and per-vaporation processes. A comparison of cross-flow, counter-flow, and counter-flow/sweep for the same membrane module used to dehydrate natural gas is shown in Figure 4.18. Water is a smaller molecule and much more condensable than methane, the main component of natural gas, so membranes with a water/methane selectivity of 400-500 are readily available. In the calculations shown in Figure 4.18, the membrane is assumed to have a pressure-normalized... [Pg.185]

Figure 4.18 Comparison of (a) cross-flow, (b) counter-flow and (c) counter-flow sweep module performance for the separation of water vapor from natural gas. Pressure-normalized methane flux 5 x 10 6cm3(STP)/cm2 s cmHg membrane selectivity, water/methane 200... Figure 4.18 Comparison of (a) cross-flow, (b) counter-flow and (c) counter-flow sweep module performance for the separation of water vapor from natural gas. Pressure-normalized methane flux 5 x 10 6cm3(STP)/cm2 s cmHg membrane selectivity, water/methane 200...
Hydrogen sulfide, water/methane Natural gas treatment Niche applications, difficult for membranes to compete with existing technology... [Pg.350]


See other pages where Water-methanal is mentioned: [Pg.49]    [Pg.64]    [Pg.25]    [Pg.35]    [Pg.97]    [Pg.176]    [Pg.114]    [Pg.21]    [Pg.3]    [Pg.3]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.6]    [Pg.16]    [Pg.507]    [Pg.409]    [Pg.64]    [Pg.478]    [Pg.118]    [Pg.157]    [Pg.27]    [Pg.186]   
See also in sourсe #XX -- [ Pg.42 ]




SEARCH



Bromo-methane water

Ethanol from hydrogen-methane-water

Hybridization in Methane, Ammonia, and Water

Hydrogen-methane-water system

Interface water-methane

Methanation water vapor effect

Methane -water interaction

Methane Content of Water in Equilibrium with Hydrates

Methane butane water system, phase

Methane in water

Methane molecules in water

Methane ocean waters

Methane pore water profiles

Methane reacting with water

Methane reaction with water

Methane solubility in water

Methane water

Methane water

Methane water radial distribution

Methane water reactions

Methane water system

Methane water versus

Temperature-Composition Diagrams for Methane Water

Water with partial methane

Water-methane mixtures

© 2024 chempedia.info