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# 3

Phase
maps
The temperatures
and pressures at
which a given
phase of a
substance is
stable (that is,
from which the
molecules have
the lowest
escaping
tendency) is an
important property
of any substance.
Because both the
temperature and pressure are factors, it is customary to plot the regions of stability of the various phases in P -
T coordinates, as in this generic phase diagram (or phase map) for a hypothetical substance.

Because pressures and temperatures can vary over very wide ranges, it is common practice to draw phase diagrams
with non-linear or distorted coordinates. This enables us to express a lot of information in a compact way and to
visualize changes that could not be represented on a linearly-scaled plot.
It is important that you be able to interpret a phase map, or alternatively, construct a rough one when given the
appropriate data. Take special note of the following points:
1. The three colored regions on the diagram are the ranges of pressure and temperature at which the correspondi ng
phase is the only stable one.
2. The three lines that bound these regions dene all values of (P,T) at which two phases can coexist (i.e., be in
equilibrium). Notice that one of these lines is the vapor pressure curve of the liquid as described above. The
"sublimation curve" is just a vapor pressure curve of the solid. The slope of the line depends on the difference in
density of the two phases.
3. In order to depict the important features of a phase diagram over the very wide range of pressures and temperatures
they encompass, the axes are not usually drawn to scale, and are usually highly distorted. This is the reason that the
"melting curve" looks like a straight line in most of these diagrams.
4. Where the three named curves intersect, all three phases can coexist. This condition can only occur at a unique
value of (P,T ) known as the triple point. Since all three phases are in equilibrium at the triple point, their vapor
pressures will be identical at this temperature.
5. The line that separates the liquid and vapor regions ends at the critical point. At temperatures and pressures greater
than the critical temperature and pressure, no separate liquid phase exists. We refer to this state simply as a fluid,
although the term supercritical liquid is also commonly used.
The best way of making sure you understand a phase diagram is to imagine that you are starting at a certain
temperature and pressure, and then change just one of these parameters, keeping the other constant. You will be
traversing a horizontal or vertical path on the phase map, and there will be a change in state every time your path
crosses a line. Of special importance is the horizontal path (shown by the blue line on the diagram above)
corresponding to a pressure of 1 atmosphere; this line defines the normal melting and boiling temperatures of a
substance.
Phase map of
Water

Notice the following features of this very
important phase diagram:

The slope of the line 2 separating the
solid and liquid regions is negative; this
reflects the unusual property that the
density of the liquid is greater than that
of the solid, and it means that the melting point of ice decreases as the pressure increases. Thus if ice at 0C is
subjected to a high pressure, it will find itself above its melting point and it will melt. (Contrary to what is sometimes
said, however, this is not the reason that ice melts under the pressure of ice skates or skis, providing a lubricating film
which makes these modes of transportation so enjoyable. The melting in these cases arises from frictional heating.)
The dashed line 1 is the extension of the liquid vapor pressure line below the freezing point. This represents the
vapor pressure of supercooled water
a metastable state of water which can temporarily exist down to about 20C. (If you live in a region subject to
"freezing rain", you will have encountered supercooled water!)
3 The triple point (TP) of water is just 0.0075 above the freezing point; only at this temperature and pressure can all
three phases of water coexist indefinitely.
4 Above the critical point (CP) temperature of 374C, no separate liquid phase of water exists.
Phase map of Carbon dioxide

Dry ice, solid carbon dioxide, is widely used as a refrigerant. The phase diagram shows why it is dry. The triple point
pressure is at 5.11 atm, so below this pressure, liquid CO2 cannot exist; the solid can only sublime directly to vapor.
Gaseous carbon dioxide at a partial pressure of 1 atm is in equilibrium with the solid at 195K (79 C, 1); this is
the normal sublimation temperature of carbon dioxide. The surface temperature of dry ice will be slightly less than
this, since the partial pressure of CO2 in contact with the solid will usually be less than 1 atm. Notice also that the
critical temperature of CO2 is only 31C. This means that on a very warm day, the CO2 in a re extinguisher will be
entirely vaporized; the vessel must therefore be strong enough to withstand a pressure of 73 atm.

This view of the carbon dioxide phase map
employs a logarithmic pressure scale and
thus encompasses a much wider range of
pressures, revealing the upper boundary of
the fluid phase (liquid and
supercritical). Supercritical carbon
dioxide (CO2 above its critical temperature)
possesses the solvent properties of a liquid
and the penetrating properties of a gas; one
major use is to remove caffeine from coee
beans.

Phase diagram of iodine
Elemental iodine, I2, forms dark gray crystals
that have an almost metallic appearance. It is
often used in chemistry classes as an
example of a solid that is easily sublimed; if
you have seen such a demonstration or
experimented with it in the lab, its phase
diagram might be of interest.
The most notable feature of iodine's phase
behavior is the very small difference (less
than a degree) between the temperatures of
its triple point 1 and melting point 2.
Contrary to the impression many people
have, there is nothing really special
which is shared by many molecular crystals including ice and naphthalene ("moth crystals".) The vapor pressure
of iodine at room temperature is really quite small only about 0.3 torr (40 Pa).The fact that solid iodine has a
strong odor and is surrounded by a purple vapor in a closed container is mainly a consequence of its strong
ability to absorb green light (this leaves blue and red which make purple) and the high sensitivity of our noses to
its vapor.
Phase diagram of sulfur
Sulfur exhibits a very complicated phase behavior that has puzzled chemists for over a century; what you see here is
the greatly simplified phase map shown in most
textbooks. The difficulty arises from the
tendency of S8 molecules to break up into
chains (especially in the liquid above 159C) or
to rearrange into rings of various sizes (S6 to
S20). Even the vapor can contain a mixture of
species S2 through S10.
The phase diagram of sulfur contains a new
feature: there are two solid
phases, rhombic and monoclinic. The names refer to the crystal structures in which the S8 molecules arrange
themselves. This gives rise to three triple points, indicated by the numbers on the diagram. [Question: which three
phases can never coexist?]
When rhombic sulfur (the stable low-temperature phase) is heated slowly, it changes to the monoclinic form at 114C,
which then melts at 119. But if the monoclinic form is heated rapidly the molecules do not have time to rearrange
themselves, so the rhombic arrangement persists as a metastable phase until it melts at 119-120.
Formation of more than one solid phase is not uncommon in fact, if one explores into the very high pressures (see
below), it seems to be the rule.

4 Phases at the extremes
We tend to think of the properties of substances as
they exist under the conditions we encounter in
everyday life, forgetting that most of the matter that
makes up our world is situated inside the Earth, where
pressures are orders of magnitude higher.
Geochemists and planetary scientists need to know
about the phase behavior of substances at high
temperatures and pressures in order to develop useful
models to test their theories about the structure and
evolution of the Earth and of the solar system.
What ranges of temperatures and pressures are likely
to be of interest and more importantly, are
experimentally accessible?

Kesetimbangan fasa dan diagram fasa
Selama ini pembahasan perubahan mutual antara tiga wujud materi difokuskan pada keadaan cair. Dengan kata lain,
perhatian telah difokuskan pada perubahan cairan dan padatan, dan antara cairan dan gas. Dalam membahas
keadaan kritis zat, akan lebih tepat menangani tiga wujud zat secara simultan, bukan membahas dua dari tiga wujud
zat.

Gambar 7.5 Diagram fasa. Tm adalah titik leleh normal air, , T3 dan P3 adalah titik tripel, Tb adalah titik didih normal,

Diagram fasa merupakan cara mudah untuk menampilkan wujud zat sebagai fungsi suhu dan tekanan. Sebagai
contoh khas, diagram fasa air diberikan di Gambar 7.5. Dalam diagram fasa, diasumsikan bahwa zat tersebut
diisolasi dengan baik dan tidak ada zat lain yang masuk atau keluar sistem.
Pemahaman Anda tentang diagram fasa akan terbantu dengan pemahaman hukum fasa Gibbs, hubungan yang
diturunkan oleh fisikawan-matematik Amerika Josiah Willard Gibbs (1839-1903) di tahun 1876. Aturan ini
menyatakan bahwa untuk kesetimbangan apapun dalam sistem tertutup, jumlah variabel bebas-disebut derajat
kebebasan F- yang sama dengan jumlah komponen C ditambah 2 dikurangi jumlah fasa P, yakni,
F=C+2-P (7.1)
Jadi, dalam titik tertentu di diagram fasa, jumlah derajat kebebasan adalah 2 yakni suhu dan tekanan; bila dua fasa
dalam kesetimbangan-sebagaimana ditunjukkan dengan garis yang membatasi daerah dua fasa hanya ada satu
derajat kebebasan-bisa suhu atau tekanan. Pada ttik tripel ketika terdapat tiga fasa tidak ada derajat kebebasan lagi.
Dari diagram fasa, Anda dapat mengkonfirmasi apa yang telah diketahui, dan lebih lanjut, Anda dapat mempelajari
apa yang belum diketahui. Misalnya, kemiringan yang negatif pada perbatasan padatan-cairan memiliki implikasi
penting sebagaimana dinyatakan di bagian kanan diagram, yakni bila tekanan diberikan pada es, es akan meleleh
dan membentuk air. Berdasarkan prinsip Le Chatelier, bila sistem pada kesetimbangan diberi tekanan,
kesetimbangan akan bergeser ke arah yang akan mengurangi perubahan ini. Hal ini berarti air memiliki volume yang
lebih kecil, kerapatan leb besar daripada es; dan semua kita telah hafal dengan fakta bahwa s mengapung di air.