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Carbon dioxide pore water

The egg shell is 94% calcium carbonate [471-34-17, CaCO, 1% calcium phosphate [7758-23-8] and a small amount of magnesium carbonate [546-93-0]. A water-insoluble keratin-type protein is found within the shell and in the outer cuticle coating. The pores of the shell allow carbon dioxide and water to escape during storage. The shell is separated from the egg contents by two protein membranes. The air cell formed by separation of these membranes increases in size because of water loss. The air cell originally forms because of the contraction of the Hquid within the egg shell when the temperature changes from the body temperature of the hen at 41.6°C to a storage temperature of the egg at 7.2°C. [Pg.456]

Extractable matter should be removed by extraction with organic solvents, e.g., xylene. This is especially important for carbon blacks (25), Oxidized carbon may contain small amounts of oxalic acid. King (33, 34) found 0.002 meq/gm of oxalic acid in oxygen-treated sugar charcoal. More severe is the contamination of the surface with adsorbed gases, mainly carbon dioxide and water. Activated carbon with narrow pores may contain considerable amounts of carbon dioxide (28). The best... [Pg.184]

The catalysts evaluated are active for synthesis gas conversion the percent conversion of H2 and CO is shown for each catalyst in Figure 1 as a function of time under evaluation conditions and temperature. At 280°C the percent conversion of synthesis gas increases with time for the acidic zeolite-supported catalysts, Fe/ZSM-5 and Fe/Mordenite, but decreases for the larger pore, non-acidic zeolite-supported catalyst Fe/13X. The percent conversion increases for all catalysts at 300°C for Fe/ZSM-5 and Fe/Mordenite the conversions remain constant at this temperature for several days, although for Fe/13X the conversion increases with time. The trends in % synthesis gas conversion, particularly % CO, are reflected in the weight % hydrocarbons, carbon dioxide and water obtained in the reactor effluent over the period of evaluation, see Figure 2. It is apparent that the catalysts are effective for the production of hydrocarbons from synthesis gas, but also catalyze the water gas shift reaction the % hydrocarbons and%C02 obtained are greater at the higher temperature (300°C) whereas the % H2O is less at this temperature than at 280°C. [Pg.400]

Once the compost mixture has been blended and formed into windrows, the volume of material will gradually decrease over time for a variety of reasons. Part of this volume decrease is due solely to the pulverization of the compost material by the windrow turner which results in smaller particle size and less pore space in the compost pile. In addition, a substantial portion of the organic matter will be respired by microorganisms to carbon dioxide and water which will then escape from the... [Pg.130]

Besides water, air is also present in soil pores, and it forms a significant part of the soil. The air penetrates into the soil from the atmosphere, however, the soil air is rather different from the atmospheric air as regards its composition. The soil air is characterized by a higher carbon dioxide and water vapour content and a lower oxygen content. The following components of the soil air are important ... [Pg.637]

The properties of fluids under supercritical conditions are considered ideal for extracting substances from exhausted activated carbons. Two supercritical fluids are of particular interest, carbon dioxide and water. Carbon dioxide has a low critical temperature of 304 K and a moderate critical pressure of 73 bar, while water has a critical temperature of 647 K and a critical pressure of 220 bar. The character of water at supercritical conditions changes from one that supports only ionic species at ambient conditions to one that dissolves paraffins, aromatics, gases and salts [65]. These supercritical fluids exhibit densities similar to those of liquids (high solvent strengths) and diffusion coefficients similar to those of gases (excellent transport characteristics), enabling them to effectively dissolve and/or desorb contaminants from the carbon surface and to easily enter/exit even the smallest pores and carry away any... [Pg.45]

Reichle et al. showed how LDH matmals are texturally modified by calcinations (389). The calcined material has an increase in both surface area and pore volume. This is a result of the formation of regularly spaced pores due to the elimination of carbon dioxide and water from the surface and the pores are both micro- and mesoporous in size. Regeneration of the LDH shows the disappearance of the micropores contributing to this increase in surface area and also a broader range of mesopore sizes. Use of organic solvent during the regeneration process produces LDHs with decreased surface areas, smaller pores, and smaller distribution of pore sizes. [Pg.421]

The physical AC preparation process involves two separate stages, the first being carbonisation, i.e. pyrolysis of the raw material at temperatures usually between 873-1073 K, in an inert atmosphere, where the pore network is developed and the non-carbon species are essentially removed. In the subsequent step of activation, the substrate is heated under an oxidizing agent (Carbon dioxide, air, water) at about 1073-1173 K. This process aims to improve the characteristics of the pore structure, e.g. increase of pore volume and surface area, tuning of the pore size etc. This step, which is a heterogeneous solid-gas reaction. [Pg.599]

Molecular sieves are available with a variety of pore sizes. A molecular sieve should be selected with a pore size that will admit H2S and water while preventing heavy hydrocarbons and aromatic compound.s from entering the pores. However, carbon dioxide molecules are about the same size as H2S molecules and present problems. Even thougli die COi is non-polar and will not bond to the active sites, the CO2 will entci the pores. Small quantities of CO2 will become trapped in the pores In this way small portions of CO2 are removed. More importantly, CO ih obstruct the access of H2S and water to active sites and decrease the eflectiveness ot the pores. Beds must be sized to remove all water and to pi ovitte for interference from other molecules in order to remove all H i.S. [Pg.161]

Components in the invading water-based filtrate and in the formation waters may react to form insoluble precipitates which can block the pores and give rise to skin damage. The scale can be formed by interaction of calcium-based brines with carbon dioxide or sulfate ions in the formation water. Alternatively sulfate ions in the invading fluid may react with calcium or barium ions in the formation water. Analysis of the formation water can identify whether such a problem may arise. [Pg.705]

Carbon dioxide is produced as a result of metabolism of all heterotrophic organisms. The concentrations of CO2 in pore water of reduced sediments are therefore high. Autotrophic microorganisms consume CO2 in the oxidized part of the sediment, which can vary in depth from a meter in deep sea sediments to a few mm... [Pg.186]

Carbon dioxide flooding is the most promising enhanced oil-recovery method. To overcome the tendency of CO2 to bypass the smaller pores containing residual oil, one approach is to plug the larger pores by chemical precipitation. Several relatively inexpensive water-soluble salts of the earth alkali group react with CO2 to form a precipitate. [Pg.229]

A series of processes will control the behaviour of C02 in saline aquifer formations. First, the C02 will displace the formation water (brine) originally in place and will lead to a local increase in pore fluid pressure (van der Meer, 1992). The injected C02 will not be distributed evenly, but will finger out, owing to the lower density than the pore waters and the heterogeneities of the aquifer. Doughty et al. (2001) point out that the shape of the C02 plume in the aquifer will be highly site- and case-specific. Carbon dioxide will rise to the top of the aquifer and migrate at the bottom of the... [Pg.179]


See other pages where Carbon dioxide pore water is mentioned: [Pg.61]    [Pg.62]    [Pg.197]    [Pg.183]    [Pg.3]    [Pg.1593]    [Pg.70]    [Pg.465]    [Pg.203]    [Pg.192]    [Pg.124]    [Pg.20]    [Pg.971]    [Pg.2009]    [Pg.266]    [Pg.287]    [Pg.198]    [Pg.204]    [Pg.395]    [Pg.290]    [Pg.513]    [Pg.1543]    [Pg.141]    [Pg.740]    [Pg.11]    [Pg.109]    [Pg.244]    [Pg.267]    [Pg.187]    [Pg.60]    [Pg.220]    [Pg.52]    [Pg.86]    [Pg.94]    [Pg.116]    [Pg.307]   
See also in sourсe #XX -- [ Pg.350 ]




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Carbon pores

Carbonated waters

Dioxide - Water

Pore waters

Water carbon dioxide

Water carbon)

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