# Vapor pressure and boiling point relationship quotes

### How do atmospheric pressure and elevation affect boiling point? | Socratic

I quote here a paragraph from Parr reactors instructions: “The loading limits How does the pressure impact the dew point of water vapor? “The relationship of total pressure (mbar) to the partial pressure (mbar) of . Safrole is a precursor of ecstasy with high boiling point and low vapor pressure at room temperature. The boiling point of a solution is generally defined as the the temperature at which the vapor pressure of a liquid is equal to the pressure of the gas above it. This relationship was used to predict the vapor pressure of liquids and good 9 At its boiling point a liquid has a vapor pressure equal to the.

It relates roughly to the average random internal kinetic energy of a system. By random I mean not correlated--a bullet moving mph has a lot of kinetic energy, but all the parts are moving at very nearly the same velocity same speed and direction.

A cup of hot tea can appear to be stationary, but each of the molecules within it can be moving at mph in a random direction. But there is more to kinetic energy than just molecules moving around translation energy. Molecules also have rotational energy, vibrational energy, and electronic energy this last one doesn't really apply unless we get to very high temperatures.

I mean, mind-bogglingly many! Imagine a pot of water with 1. It contains more than 6x molecules of water that's about a million times as many stars as there are in the visible universe So one can easily confuse themselves by going back and forth between thinking about bulk properties like temperature and individual molecules, or small numbers of molecules like less than a few trillion.

The best way to avoid these confusions is to think about distributions https: This distribution describes the proportion of molecules in each state speed.

## Translation

And because there are so freakin many molecules, even the most bizarre things happen. If we add a little heat, some ice melts. Remove a little heat and some water freezes. We call this the equilibrium freezing temperature: More about supercooling and super heating below.

An aqueous solution has a higher boiling point and a lower freezing point than does pure water. If the solution is not too concentrated, these two effects are approximately independent of what the dissolved substance is: So, provided you remember to count each ion separately, the effect of concentration on boiling point elevation or freezing point depression is much the same for all small solutes in water.

Macromolecules such as polymers behave differently because they have lots of neighbouring solvent molecules, and so affect the solvent much more than simple solutes. So, you might expect that the antifreeze in a radiator not only stops it freezing, but also helps stop it from boiling. However, the real situation is more complicated: Ethylene glycol is one antifreeze. Salt is used to melt snow and ice on roads in cold countries, but it is not used in radiators because it is corrosive and crystallises readily.

Sugar is not used in some applications, because concentrated sugar solutions are viscous, and because they support bugs. However, many organisms use sugars and other small organic molecules as antifreeze. The concentration of solutes in blood is less than that in sea water, so the equilibrium freezing temperature of blood is usually higher than that of sea water.

Consequently, some Arctic and Antarctic fish live at temperatures below the equilibrium freezing temperature of normal blood.

The bio-antifreeze in their blood is a protein that works in a way different from the anti-freeze used in car radiators: The effect of pressure Notice that above I've included the proviso "at atmospheric pressure" a few times. The reason why the pressure is important is that, in the vapour phase, a given amount of a substance occupies a much larger volume than it does as a liquid.

Some of the energy required to vapourise it goes towards 'pushing the air out of the way' to make room for the amount evaporated. So, at low pressure, it is easier to form the vapour phase and so the boiling point is lower. The dependence of the transition temperature on pressure is the Clausius-Clapeyron effect.

Again, being a bit technical, we note that this effect involves energy - the work done in displacing air - whereas the solute effect involves entropy - the disordering of the liquid phase. Water expands a lot when it boils: This means that even modest increases in altitude can measurably reduce the boiling temperature.

Some people complain that this affects cooking and even the taste of tea at altitude. It is also true that pressure changes the melting temperature. However, because the volume occupied by a kilogram of liquid is not much different from that occupied by a kilogram of solid, this effect is very small unless the pressures are very large.

For most substances, the freezing point rises, though only very slightly, with increased pressure. Water is one of the very rare substances that expands upon freezing which is why ice floats.

Consequently, its melting temperature falls very slightly if pressure is increased.

### What does vapor pressure mean?

I have been asked: Does freezing point depression with pressure explain the low friction under an ice-skate? I'm writing this in Sydney, so you might guess correctly that I don't know much about skating, but let's try to be quantitative. The Clausius-Clapeyron equation says that the ratio of the change in pressure times the change in specific volume to the latent heat of the phase change equals the ratio of the change in transition temperature to the absolute melting or boiling temperature.

As we might have guessed from dimensional considerations — i. The weight of the skater is say 1 kN.

### The chemical elements of the periodic table sorted by boiling point

I'm not a skater, but let's start with an estimate of the skate-ice contact area as say mm2. The value depends on how far the skate cuts into the ice. Say mm long by 0. A kg of water one litre freezes to give about 1. So, with this estimate for area and if this were the cause of the slipperiness, ice skating would be possible only at temperatures only one or a few degrees below freezing.

From observation, it is possible to ice skate on ice at much lower temperatures than this. If only the sharp edges were in contact with the ice, this might be possible, but it seems very low to me, because I'd expect the edges to cut into the ice and to increase the area of contact. Again, I seek advice from skaters on this, and preferably from physicists who are also skaters. Putting aside the Clausius-Clapeyron effect, and under conditions with only small applied pressure, we'd expect the surface of ice is already somewhat slippery.

At the surface of ice, water molecules are only have opportunities for hydrogen bonds to their neighbours 'on one side', as it were. Consequently, their energy is not as low as in bulk ice. So, at equilibrium, they must have a higher entropy.