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Water-point

Salt Brines The typical curve of freezing point is shown in Fig. II-IIO. Brine of concentration x (water concentration is I-x) will not solidify at 0°C (freezing temperature for water, point A). When the temperature drops to B, the first ciystal of ice is formed. As the temperature decreases to C, ice ciystals continue to form and their mixture with the brine solution forms the slush. At the point C there will be part ice in the mixture /(/i+L), and liquid (brine) /i/(/i-t-L). At point D there is mixture of mi parts eutectic brine solution Di [concentration mi/(mi-t-mg)], and mo parts of ice [concentration mol m -t- mo)]. Coohng the mixture below D solidifies the entire solution at the eutectic temperature. Eutectic temperature is the lowest temperature that can be reached with no solidification. [Pg.1124]

A salt hydrate consists of two components, the salt (e.g. CaCL) and water (e.g. 6H2O). The single phase of the salt hydrate is first heated up from point 1 (solid) to point 2. At point 3 the liquidus line is crossed and the material would be completely liquid. Upon heating or cooling, between point 2 and 3,2 phases are formed, the liquid and a small amount of a phase with less water (point 4). If these phases differ in density, this can lead to macroscopic separation of the phases and therefore concentration differences of the chemicals forming the PCM material (points 5 and Figure 104 right). [Pg.265]

Chelli R, Barducci A, Bellucci L, Schettino V, Procacci P (2005) Behavior of polarizable models in presence of strong electric fields. I. Origin of nonlinear effects in water point-charge systems. J Chem Phys 123(19) 194109... [Pg.252]

Fig. 12.3 The covalent radii and ionic radii inNaCl crystals and in aqueous solutions, the hydration bond lengths, d( 0) from the ion/water point of contact, P(i/w) to the center of O of water and the length of the hydrogen bon, d(--H) with Cl ... Fig. 12.3 The covalent radii and ionic radii inNaCl crystals and in aqueous solutions, the hydration bond lengths, d( 0) from the ion/water point of contact, P(i/w) to the center of O of water and the length of the hydrogen bon, d(--H) with Cl ...
Some authors have claimed that their system survived as microemulsions almost down to the 100% water point on the triple-phase diagram. Unfortunately this claim does not appear to be substantiated by the published phase diagrams and the claim... [Pg.200]

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.)...
Figure 6. The linear range of the ionization constants of the acids vs. the dielectric constant function at 25°C. ethanol-water (O) methanol-water (A) 2-methoxyethanol-water dioxane-water (D) acetone-water, glycerol-water, 2-propanol-water ( ). Points owing to tetrahydrofuran-water, 2-ethoxyethanol-water, and 1,2-dimethoxyethane-water systems are not shown on the plots they all lie on the linear plots. Figure 6. The linear range of the ionization constants of the acids vs. the dielectric constant function at 25°C. ethanol-water (O) methanol-water (A) 2-methoxyethanol-water dioxane-water (D) acetone-water, glycerol-water, 2-propanol-water ( ). Points owing to tetrahydrofuran-water, 2-ethoxyethanol-water, and 1,2-dimethoxyethane-water systems are not shown on the plots they all lie on the linear plots.
Access and water supply. All people have safe access to a sufficient quantity of water for drinking, cooking, and personal and domestic hygiene. Public water points are sufficiently close to households to allow use of the minimum water requirement. [Pg.184]

The maximum distance from any household to the nearest water point is 500 meters. [Pg.184]

The b.p. usually increases with the atomic weight of the element combined with hydrogen, but the large deviations shown by hydrofluoric add and water point to association of these compounds, which is confirmed in many other ways. By a comparison of the b.ps. of hydrocarbonsi Vernon concluded that... [Pg.302]

Fig. 1.11. Dependence oC retention factors, k. of homologous -alkylbcnrcncs on the number ol carbon atoms. i. in the alkyl group on a Silasorb SPH C x 7.5 im) column t. (X) x 4.0 mm i.d.) in mobile phases containing 60 (/), 65 (2). 70 (.f). 80 (4) and 901.5> A vol. methanol in water. Points experimental data lines best plots of Eq. (1.19) w-ith the quadratic term equal to 0. Fig. 1.11. Dependence oC retention factors, k. of homologous -alkylbcnrcncs on the number ol carbon atoms. i. in the alkyl group on a Silasorb SPH C x 7.5 im) column t. (X) x 4.0 mm i.d.) in mobile phases containing 60 (/), 65 (2). 70 (.f). 80 (4) and 901.5> A vol. methanol in water. Points experimental data lines best plots of Eq. (1.19) w-ith the quadratic term equal to 0.
Littoral—The part of the benthic realm between high and low water points. [Pg.639]

Figure 3. Point-source map showing the distribution of arsenic in Bangladesh well waters. Points in red are wells with greater than the Bangladesh standard for arsenic in drinking water (50 pg LT)... Figure 3. Point-source map showing the distribution of arsenic in Bangladesh well waters. Points in red are wells with greater than the Bangladesh standard for arsenic in drinking water (50 pg LT)...
The appearance of simple phenolic compounds in water points to pollution stemming from industrial sources, such as manufacturers of dyes, drugs, antioxidants, pulp and paper, or may be the result of pesticide application. The presence of certain phenols in... [Pg.920]

Have teams pick up their materials. Then focus students attention on the small plastic cup of water. Point out that it is marked with five different measurement units and explain that the class will be using the milliliter (ml) unit during this test. [Pg.63]

He shows that pure water at normal pressures cannot be supercooled below -40°C and that virtually all physical properties of water point to a "lambda anomaly" at -45 C [1]. [Pg.4]

Wells and natural watering points on streams and rivers,... [Pg.12]

Fig. 8.4. Entropy versus pressure for water. Points A and B correspond to Figure 8.1. Fig. 8.4. Entropy versus pressure for water. Points A and B correspond to Figure 8.1.

See other pages where Water-point is mentioned: [Pg.43]    [Pg.182]    [Pg.402]    [Pg.106]    [Pg.151]    [Pg.184]    [Pg.1230]    [Pg.644]    [Pg.2382]    [Pg.104]    [Pg.271]    [Pg.473]    [Pg.268]    [Pg.270]    [Pg.430]    [Pg.108]    [Pg.5]    [Pg.29]    [Pg.398]    [Pg.91]    [Pg.83]    [Pg.26]    [Pg.12]    [Pg.445]   
See also in sourсe #XX -- [ Pg.97 ]




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Boiling point of water

Boiling point of water at various pressures

Critical point of water

Determining the Freezing Point of Water

Dew-Point Method for the Determination of Water Activity

Ethanol-water mixtures, freezing point

Ethylene glycol-water mixtures, freezing point

Freezing Points of Ethyl Alcohol-Water Mixture

Freezing Points of Hexylene Glycol-Water Mixtures

Freezing point of water

Ground water point source origins

Melting point of water

Methanol-water mixtures, freezing point

Nonionic Surfactant and Water Cloud Point

Point sources water scarcity

Point sources, water pollution

Simple point charge extended water model

Simple point charge model, water

Triple point constants water

Triple point of water

Water Vapor Dew Points Over Aqueous Ethylene Glycol Solutions

Water boiling point elevation constant

Water boiling points

Water boiling-point elevation

Water critical point

Water dew point

Water equilibrium freezing point

Water fixed point properties

Water freezing point

Water freezing point depression constant

Water freezing point, pressure dependence

Water freezing-point depression

Water melting point

Water molal boiling-point-elevation constant

Water molal freezing-point depression

Water point group

Water point-charge models

Water releases point sources

Water triple point

Water, amide reactions boiling point

Water, boiling point dissociation constant

Water, boiling point ionic product

Water, critical point, temperature

Water, density triple point

Water, glass point

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