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Water critical

The critical points in these mixtures are all at pressures higher than the critical pressure of water many are at temperatures higher than the water critical temperature. The mixture critical points indicate that high density phase separations persist to extreme conditions of temperature and pressure. [Pg.386]

Figure 3 The phase diagram of water. Critical temperature and pressure of light water, H2O, are 374 C and 22.1 MPa. Figure 3 The phase diagram of water. Critical temperature and pressure of light water, H2O, are 374 C and 22.1 MPa.
The most difficult aspect of estimating indirect photoreaction rates is finding a measured value of koX or estimating koX for the oxidant and compound of interest. Measured values of koX are usually much preferred to estimated values, but measured values are available only for a small proportion of organic compounds likely to be found in surface waters. Critical compilations of rate constants for oxidant reactions with organic compounds in water appear in Hendry et al. (RO, R02) (1974) Wilkinson et al. (J02) (1995) Buxton et al. (HO and e Aq) (1988) Hendry and Schuetzle (HOz) (1976) Neta et al. (R02) (1990) and Haag and Yao (HO) (1992). [Pg.391]

Water Critical pressure and temperature values of water are 220 bar and 373.14 °C. Steam is a valuable heating agent below 200 °C, where the saturation pressure is about 24 bar. Superheated steam can be used to enlarge the temperature range. Liquid water is excellent for cooling, but also for heating at mild temperatures below 100 °C. For higher temperatures thermal fluids are more suitable. [Pg.474]

After the numbers of nuclei have been determined, the fluorochrome is added to the nuclei. A staining concentration of 2.5 pig of DAPI per 106 nuclei (determined by a titration curve) is used. The stock solution of DAPI consists of 1 pig of DAPI per 1 pi of distilled water. Critical to proper staining is the accurate determination of the number of nuclei to be stained (fluorochrome nuclei ratio). This caveat should be heeded with all fluorochromes. The titration curve of DAPI is such that significant over- as well as underestimates of the number of nuclei result in distortions of the resulting data. Similar results, although not so extreme, have been observed with other fluorochromes. After staining, the samples are kept on ice until examined. [Pg.207]

Gaseous Water—Critical Constants—Laient Heat of Vaporisation —Sjieeilie Heat. [Pg.386]

USEPA (1998) Oxygenates in Water Critical Information and Research Needs. EPA-600-R-98/048. Office of Research and Development, Washington, DC... [Pg.29]

USEPA (1998) Oxygenates in water critical information and research needs. Report... [Pg.328]

An article in Chemical cmd Engineering News (Sept. 28, 1987) descn bes a hydrothermal autoclave. This device is of constant volume, is evacuated, and then water is added so that a fraction. r of the total volume is filled with liquid water and the remainder is filled with water vapor. The autoclave is then heated so that the temperature and pressure in the sealed vessel increase. It is observed that if x is greater than a critical fill value, x, the liquid volume fraction increases as the temperature increases, and the vessel becomes completely filled with liquid.at temperatures below the critical temperature. On the other hand, if. c < Xc, the liquid evaporates as temperature is increased, and the autoclave beconres completely filled with vapor below the water critical temperature. If, however, x = Xc, the volume fraction of liquid in the autoclave remains constant as the temperature increases, and the temperature-pressure trajectory passes through the water critical point. Assuming the. hydrothermal autoclave is to be loaded at 25° C, calculate the critical fiU Xc... [Pg.329]

Values directly below undescored viscosities are for water. Critical point. [Pg.351]

H. F. Eicke and H. Christen, Is water critical to the formation of micelles in apolar media ,... [Pg.186]

Figure 3. ITie dielectric constant of water along the 25 MPa isobar (a) as a function of temperature, where there is a steep drop just above the water critical temperature (b) as a function of density, where the decrease is gradual. Figure 3. ITie dielectric constant of water along the 25 MPa isobar (a) as a function of temperature, where there is a steep drop just above the water critical temperature (b) as a function of density, where the decrease is gradual.
Figure 9. Schematic plot of critical lines of some Type-III, and also of some Type-1 aqueous systems near the water critical point. The cross-hatches indicate on which side of the critical line the system exists in two phases. (Reprinted from 12] Fig. 11, copyright 1994, with kind permission from Kluwer Academic Publishers)... Figure 9. Schematic plot of critical lines of some Type-III, and also of some Type-1 aqueous systems near the water critical point. The cross-hatches indicate on which side of the critical line the system exists in two phases. (Reprinted from 12] Fig. 11, copyright 1994, with kind permission from Kluwer Academic Publishers)...
Figure 17. llie isochoric heat capacity of 1 weight % of sodium sulfate in water, at a density near the water critical density, as a function of temperature (Reprinted from [27J, Fig. 3, Copyright 1998, with permission from Elsevier Science). Figure 17. llie isochoric heat capacity of 1 weight % of sodium sulfate in water, at a density near the water critical density, as a function of temperature (Reprinted from [27J, Fig. 3, Copyright 1998, with permission from Elsevier Science).
Two of the group 16 elements—oxygen and sulfur—are among the most familiar ones. Not only is water critical to all life and O2 to all aerobic life, the ozone layer protects life and civilization on Earth from the sun s harmful ultraviolet rays. The annual worldwide production of sulfuric acid is in the hundreds of millions of metric tons and is the highest by weight for all industrial chemicals. Indeed, the amount of sulfuric acid produced is often a good indicator of a country s state of industrial development and economic status. [Pg.202]

Spent fuel elements from power reactors are stored under water. Criticality calculations on the storage arrays must assume an Infinite lattice since large numbers of elements are usually present. About 12 to 14 in. of water between fuel elements reduces neutron interaction currents to zero. In this case the array is critical only if individual elements are also critical. Appreciable interaction currents are required for array criticality when the individual elements are far from critical alone. This suggests that safe lattice separations can be expressed in terms of the kgff of isolated fuel elements. [Pg.202]

J. D. CHALMERS, Criticality Parameters for Mixtures of Plutonium Oxide, Uranium Oxide and Water, Criticality Control of Fissile Material, pp. 3-11, International Atomic Energy Agency, Vienna (1966). [Pg.324]

Limits will be provided for both dry aind water-moderated systems. A completely dry oxide system inay be difficult to guarantee hence, limits will also be provided for damp [H/(U + Pu) <0.45] oxide. Solutions and slurries are assumed to be uniform, homogeneous mixtures of UO, (10.96 g/cm ) and PuOb (11.46 g/cm for PuQ ) in water. Critical dimensions of such systems have minima as a function of concentration, provided the oxide mixture does not contain much more than 30% PuO by weight. [Pg.428]

No. GRID NUMBER OF ROLES ROi column WATER CRITICAL HEIGHT (mm)... [Pg.588]

Ctleulated Keff Values for Cylindrical Rod-Water Critical Lattices (2,70 wt% > U Scalnless-Steel-Oad UO2 Rods)... [Pg.591]

Positive deviations to the DHLL are observed for strongly associated electrolytes as MgS04 at moderate temperatures or NaCl close to the water critical temperature. The reason of the deviation is the reduction of the electrostrictive effect when ion-pairs are formed, which leads to an expansion of the solution. [Pg.142]


See other pages where Water critical is mentioned: [Pg.513]    [Pg.57]    [Pg.255]    [Pg.492]    [Pg.293]    [Pg.62]    [Pg.190]    [Pg.25]    [Pg.167]    [Pg.109]    [Pg.593]    [Pg.514]    [Pg.257]    [Pg.70]    [Pg.298]    [Pg.317]    [Pg.35]    [Pg.34]    [Pg.27]    [Pg.369]    [Pg.837]    [Pg.73]    [Pg.643]    [Pg.153]   
See also in sourсe #XX -- [ Pg.60 ]




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Critical enhancements water

Critical liquid water formation

Critical point of water

Critical pressure of water

Critical solution temperature application to determination of water

Critical solution temperature, phenol-water

Critical solution temperature, phenol-water systems

Critical temperature of water

Critical water activity

Critical water concentration

Critical water content

Critical water cut

Dynamics Simulation of Water at Critical and Supercritical Conditions

Extraction near-critical/supercritical water

Green solvents near-critical” water

High Temperature, Superheated or Near Critical Water

Near-critical water

Near-critical water chemical synthesis

Near-critical water materials synthesis

Sub-critical water

Super critical water oxidation

Supercritical water oxidation critical temperature

Surface critical behavior of water

Water Critical relative humidity

Water critical constants

Water critical data

Water critical lines

Water critical point

Water critical pressure

Water critical pressure ratio

Water critical temperature

Water, critical point, temperature

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