Vapor pressure, lowering

Poly(alkylene glycol)s have a number of characteristics that make them desirable as lubricants. Compared to petroleum lubricants, they have lower pour points, a higher viscosity index, and a wider range of solubilities including water, compatibility with elastomers, less tendency to form tar and sludge, and lower vapor pressure (35). 

Organic compounds of bromine usually resemble their chlorine analogues but have higher densities and lower vapor pressures. The bromo compounds are more reactive toward alkaUes and metals brominated solvents should generally be kept from contact with active metals such as aluminum. On the other hand, they present less fire hazard one bromine atom per molecule reduces flammabiUty about as much as two chlorine atoms. 

Increased partial pressure due to reaction. An example is the reaction of SO3 and H9O to yield H9SO4, which has much lower vapor pressure than its components. 

The rate of release, in the event of loss of containment, will be reduced because of the lower vapor pressure in the event of a leak. 

Changing to a fluid with a lower vapor pressure. 

Change to another more expensive solvent, which by virtue of its lower vapor pressure would emit less organic matter. 

A general description of the three major classes of MDI s and brief descriptions of adhesive applications are shown in Table 1. More recently, MDl has become the isocyanate of choice in adhesives, partly because MDI has a lower vapor pressure than TDI does (see pp. 296-297 in [18]). Isocyanates have been shown to cause an allergic reaction in a small percentage of the population. This reaction can manifest itself in the form of an asthmatic condition [19]. Before starting work with isocyanates, researchers are encouraged to read about the proper precautions to take, in order to work safely with these materials. Researchers should also check with their local health and environmental safety representatives [20]. 

Two sources of absorption oil are normally utilized in this tower. The first is the hydrocarbon liquid from the main fractionator overhead receiver. This stream, often called wild, or unstabilized, naphtha, enters the absorber a few trays below the top tray. The second absorbent is cooled debutanized gasoline, which generally enters on the top tray. It has a lower vapor pressure and can be considered a trim absorbent. The expression lean oil generally refers to the debutanized gasoline plus the unstabilized naphtha from the overhead receiver. 

Reformulated gasoline specifications require lower vapor pressure in the blended gasoline. It also requires maximum feed to the alkylation unit. This puts more pressure on the gas plant, particularly the debutanizer. Floating the tower pressure is often the best way to meet both constraints. 

In the discharged state of ZEBRA batteries NaCl is formed in the positive electrode, which is beside the NaAlCl4. In abuse experiments, e.g., overheating, less volatile material will be released in the discharged state compared with the charged state where no NaCl is present. This is due to the lower vapor pressure of mixtures with increased NaCl content. 

Ionic compounds typically have higher boiling points and lower vapor pressures than covalent compounds. Predict which compound in the following pairs has the lower vapor pressure at room temperature (a) CEO or Na,0 (b) InCl, or SbCl, (c) LiH or HC1 (d) MgCl, or PCI,. 

STRATEGY Expect a lower vapor pressure when the solute is present. Calculate the mole fraction of the solvent (water) in the solution and then apply Raoult s law. To use Raoult s law, we need the vapor pressure of the pure solvent (Table 8.2 or 8.3). 

FIGURE 8.28 The vapor pressure of a solvent is lowered by a nonvolatile solute. The barometer tube on the left has a small volume of pure water floating on the mercury. That on the right has a small volume of 10 m NaCI(aq) and a lower vapor pressure. Note that the column on the right is depressed less by the vapor in the space above the mercury than the one on the left, showing that the vapor pressure is lower when solute is present. 

Alcohols with low molar masses are liquids, and alcohols have much lower vapor pressures than do hydrocarbons with approximately the same molar mass. For example, ethanol is a liquid at room temperature, but butane, which has a higher molar mass than ethanol, is a gas. The relatively low volatility of alcohols is a sign of the strength of hydrogen bonds. The ability of alcohols to form hydrogen bonds also accounts for the solubility in water of alcohols with low molar mass. 

To show you that compounds with higher AH s have lower vapor pressures. This means that it takes more energy to vaporize them. 

As an example, suppose you were to try to directly distill quinoline. Quinoline has a boiling point of 237°C at 1 atm. Heating organic molecules to these temperatures may often be a way to decompose them. Fortunately, quinoline is insoluble in water and it does have some vapor pressure at about the boiling point of water (10 torr at 99.6° C). If it had a much lower vapor pressure at the boiling point of water, (say 0.1 torr), there wouldn t be enough of it vaporizing to make even steam distillation worthwhile. 

Organophosphates (Fig. 10, Table 3) are more toxic than chlorinated hydrocarbons, in particular to humans,but they exhibit lower persistence in soils and do not seem to accumulate in soil fauna or concentrate in birds and fish [74]. This behavior is also related to an enhanced water solubility and lower vapor pressure of organophosphates. Malathion and Parathion (Fig. 10, Table 3) insecticides are known to be chemically hydrolyzed and biodegraded by micro-... 

The activity of the solvent often can be obtained by an experimental technique known as the isopiestic method [5]. With this method we compare solutions of two different nonvolatile solutes for one of which, the reference solution, the activity of the solvent has been determined previously with high precision. If both solutions are placed in an evacuated container, solvent will evaporate from the solution with higher vapor pressure and condense into the solution with lower vapor pressure until equilibrium is attained. The solute concentration for each solution then is determined by analysis. Once the molality of the reference solution is known, the activity of the solvent in the reference solution can be read from records of previous experiments with reference solutions. As the standard state of the solvent is the same for all solutes, the activity of the solvent is the same in both solutions at equUibrium. Once the activity of the solvent is known as a function of m2 for the new solution, the activity of the new solute can be calculated by the methods discussed previously in this section. 

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