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Water boiling point elevation

The coUigative properties of antifreeze chemicals may also result in boiling point elevation. As the chemical is added to water, the boiling point of the mixture increases. Unlike the freeze depression, the boiling elevation does not experience a maximum the boiling point versus concentration curve is a smooth curve that achieves its maximum at the 100% antifreeze level. The boiling point elevation can be another important characteristic for antifreeze fluids in certain heat-transfer appHcations. [Pg.186]

When the concentration of sugar reaches 66%, you are at the maple syrup stage. The calculated boiling point elevation (660 g of sugar, 340 g of water)... [Pg.278]

Hence the water in the solution freezes at —0.2°C. A similar expression (boiling-point elevation = kb X molality) is used to relate the elevation of boiling point to the molality of the solute. [Pg.454]

A = Kj- Cflj A 7b = Ki) Cflj We use molality in these equations because they describe temperature changes. The constant Zf is called the freezing point depression constant, and is called the boiling point elevation constant. These constants are different for different solvents but do not depend on the identity of the solutes. For water, Zf is 1.858 °C kg/mol and is 0.512 °C kg/mol. [Pg.860]

The table above shows the effects of various solutes in a given volume of water. Without knowing the acmal values, which of these is the most likely reason that the Na2C03 will cause the greatest boiling point elevation ... [Pg.29]

What is the evaporation rate and yield of the sodium acetate hydrate CH3C00Na.3H20 from a continuous evaporative crystalliser operating at 1 kN/m2 when it is fed with 1 kg/s of a 50 per cent by mass aqueous solution of sodium acetate hydrate at 350 K The boiling point elevation of the solution is 10 degK and the heat of crystallisation is 150 kJ/kg. The mean heat capacity of the solution is 3.5 kJ/kg K and, at 1 kN/m2, water boils at 280 K at which temperature the latent heat of vaporisation is 2.482 MJ/kg. Over the range 270-305 K, the solubility of sodium acetate hydrate in water s at T(K) is given approximately by ... [Pg.232]

B. In the equation At = i m - Kb, where At is the boiling-point elevation, m is the molality of the solution, and Kb is the boiling-point-elevation constant for water, i (the van t Hoff factor) would be expected to be 4 if H3B03 were completely ionized. According to data provided, i is about 1.5. Therefore, H3B03 must have a relatively low Ka. [Pg.31]

IQ = molal freezing-point depression constant Kb = molal boiling-point elevation constant Kf for water = 1.86 K kg mol-1 for water = 0.512 K kg mol-1 AT = iKf x molality ATb = iKb x molality n = MRT... [Pg.368]

At 13.5 kN/m2, water boils at 325 K and, in the absence of data on the boiling point elevation, this will be taken as the temperature of evaporation, assuming an aqueous solution. The total enthalpy of steam at 325 K is 2594 kJ/kg. [Pg.779]

What is the boiling point of a solution containing 158 g of sodium chloride (NaCl) and 1.2 kg of water What if the same number of moles of calcium chloride (CaCl2) is added to the solvent instead Explain why there s such a great difference in the boiling point elevation. [Pg.188]

Adding an impurity to a solvent makes its liquid phase more stable through the combined effects of boiling point elevation and freezing point depression. That s why you r irely see bodies of frozen salt water. The salt in the oceans lowers the freezing point of the water, making the liquid phase more stable and able to sustain temperatures slightly below 0°C. [Pg.189]

If you instead add the same number of moles of calcium chloride (2.71 mol) to the water, the calcium chloride would dissociate into three particles per mole in solution. This gives you 2.71 molx3 = 8.13 mol of solute in solution. As with the sodium chloride solution, divide the number of moles by the mass of solvent (1.2 kg) to get 6.8 m, and multiply by the of water (0.512°C/m) to get a of 3.5°C. This is a difference of more than 1 degree The difference arises because colligative properties such as boiling point elevation depend on only the number of particles in solution. [Pg.193]

ACTIVITY COEFFICIENT. A fractional number which when multiplied by the molar concentration of a substance in solution yields the chemical activity. This term provides an approximation of how much interaction exists between molecules at higher concentrations. Activity coefficients and activities are most commonly obtained from measurements of vapor-pressure lowering, freezing-point depression, boiling-point elevation, solubility, and electromotive force. In certain cases, activity coefficients can be estimated theoretically. As commonly used, activity is a relative quantity having unit value in some chosen standard state. Thus, the standard state of unit activity for water, dty, in aqueous solutions of potassium chloride is pure liquid water at one atmosphere pressure and the given temperature. The standard slate for the activity of a solute like potassium chloride is often so defined as to make the ratio of the activity to the concentration of solute approach unity as Ihe concentration decreases to zero. [Pg.29]

For certain liquids, tile temperature of a boiling solution of the unknown may be compared with that of boiling water at the same pressure, For a given solution, the boiling-point elevation may be calibrated in terms of specific gravity at standard temperature. Usually two resistance thermometers are used. The system finds use in the control of evaporators to determine the endpoint of evaporation, Good accuracy is achieved in the determination of one dissolved component, or of mixtures of fixed composition. [Pg.1530]

Before proceeding to use this equation some consideration must be given to the boiling point elevation of sodium chloride solutions. This varies with concentration and with temperature level. Because somewhat conflicting values have appeared in some of the recent literature on saline-water conversion, it seems desirable to digress for a moment to give the basis for the present values. The International... [Pg.15]

Heat of Concentration and Boiling Point Elevation of Sea Water... [Pg.24]

Values of the heat of concentration and heat capacity of sea water near room temperature have been measured experimentally. The heat of concentration values compare favorably with those calculated from the vapor pressure data given by Arons and Kientzler by use of the Clapeyron equation. The heat capacity agrees with tne values reported by Cox and Smith. Calculated values for the heat of concentration and boiling point elevation from 77° to 302° F. at salinities up to 9% are presented in both tabular and graphical form. [Pg.24]

Even with this unequal distribution there may be little effect on yield of distillate from a substantially fresh water feed hence the high output of the still from distilled water feed. With sea water, 3 to 4% NaCl equivalent, the average or effective boiling point elevation becomes unequal on the two rotors. Thus if a 50% cut is secured and the lower rotor receives twice the feed of the upper, the average residue concentrate of 7% brine from 3.5% feed could be an actual 10% from the upper periphery and 5% from the lower, supposing equal rates of distillation. Actually because of -the different elevations of boiling point (1.1° and 1.8° F.) the rate of evaporation from the upper rotor decreases while that from the lower rotor increases but less than proportionally because of the added thickness of the feed layer. Later experiments at Columbus on the No. 4 machine suggest that this situation existed in the No. 5 still. [Pg.136]

The boiling-point elevation of a solution relative to that of a pure solvent depends on the concentration of dissolved particles, just as vapor-pressure lowering does. Thus, a 1.00 m solution of glucose in water boils at 100.51°C at 1 atm pressure (0.51°C above normal), but a 1.00 m solution of NaCl in water boils at... [Pg.450]

What is the molality of an aqueous glucose solution if the boiling point of the solution at 1 atm pressure is 101.27°C The molal boiling-point-elevation constant for water is given in Table 11.4. [Pg.452]

The Boiling-Point Elevation and Freezing-Point Depression activity (eChapter 11.7) illustrates how the boiling point and freezing point of water are affected by the addition of different solutes. [Pg.470]

Concentrations expressed as molality or mole fractions are temperature-independent and are most useful when a physical measurement is related to theory over a range of temperature, e.g., in freezing point depression or boiling point elevation measurements (Chapter 11). Since the density of water is close to 1 g/cm3, molal and molar concentrations are nearly equal numerically for dilute aqueous solutions (<0.1 M). [Pg.41]

The importance of M is unmistakable when it is recalled that 180 g glucose in 10s g water [1 molal (m)] lowers the freezing point by 1.86°C, whereas the same weight of polysaccharide (1.80 X 10 3 m, assuming M = 105 g) has no such effect and, moreover, it is difficult if not impossible to disperse 105 g of any polysaccharide in 103 g water. Identical arguments hold for boiling-point elevation and osmotic pressure. However, polysaccharides at much lower concentrations exercise influences, most prominently by... [Pg.5]


See other pages where Water boiling point elevation is mentioned: [Pg.560]    [Pg.560]    [Pg.245]    [Pg.1668]    [Pg.41]    [Pg.693]    [Pg.325]    [Pg.293]    [Pg.430]    [Pg.261]    [Pg.129]    [Pg.132]    [Pg.26]    [Pg.107]    [Pg.42]    [Pg.43]    [Pg.432]    [Pg.416]    [Pg.15]    [Pg.122]    [Pg.133]    [Pg.136]    [Pg.208]    [Pg.208]   
See also in sourсe #XX -- [ Pg.534 ]

See also in sourсe #XX -- [ Pg.119 ]




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