badai
badai
11-Apr-16
Kimia Air
Formula H2O
Wujudnya dalam cair, padat dan uap
Struktur molekul air unik dengan atom
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1. Tegangan permukaan
A meniscus forms (left) when hydrogen atoms reach upward to wet oxide surfaces of the
glass tube at the water line. The drawing at the right shows how hydrogen bonding of water
to a thin glass tube causes water in the tube to rise above the level of the surrounding
water.
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Elektrolit:
Bila mineral-mineral terlarut dalam air, akan membentuk
kation dan anion.
Pada umumnya, bila suhu air meningkat menyebabkan
kelarutan garam-garam seperti NaCl dan K2SO4 semakin
bertambah. Namun akan berbeda untuk CaCO3; CaSO4;
MgCO3 dan Mg(OH)2 yang akan sulit larut meskipun suhu air
bertambah.
Elektrolit:
A simple demonstration of ionization is an experiment in which an electric light is
connected to a circuit with two separated electrodes inserted in a beaker of water (see
Fig.).
In pure water, the lamp does not light when the switch is on, because pure water is an
insulator not a conductor. Salt is added to the water in small increments, and gradually
the light brightens. The light intensity is proportional to the amount of salt added.
Current begins to flow only after sodium and chloride ions from the salt are present to
transport electrons through the solution. If crystals of sugar are added to the water
instead of salt, nothing happens; salt is an electrolyte, and sugar is not. Sugar is a
polar organic compound that does not dissociate into ions when it dissolves.
Solubility of some minerals increases with temperature (direct solubility) while other minerals have
decreasing solubility with increasing temperature (inverse solubility).
Pure water is nonconductive, but addition of an ionizing salt allows current to pass
Elektrolit:
High concentrations of impurities are known to lower the freezing point of water. For
example, 1 mol/L of a nonelectrolyte such as sugar or alcohol dissolved in water lowers
the freezing point by 3.35F (1.86C). However, 1 mol/L of sodium chloride lowers the
freezing point by almost twice the value found for sugar and alcohol, and 1 mol/L of
sodium sulfate produces almost three times this temperature depression. This is due to
the production of multiple ions in solution from the salts, compared to only one
dissolved molecule from sugar or alcohol. Each molecule of sodium chloride produces
two ions, and one molecule of sodium sulfate (Na2SO4) produces three ions.
Elements in specific groups of the periodic chart become either cations or anions,
depending on the group of elements.
Electromotive Series:
In their elemental form, alkali metals and alkaline earth metals can displace hydrogen
from aqueous solutions.
Sodium and potassium are so active that they react with water itself to liberate
hydrogen:
2Na + 2H2O H2 + 2NaOH
Magnesium does not react with cold water, but it does react with acid, which releases
hydrogen in a solution:
Mg + 2HCl H2 +MgCl2
Cations can be classified according to their reactivity in an order known as the
electromotive series, shown in following Table. Not only will the more reactive metals
displace hydrogen from solution, but they will even displace metals below them in the
series. For example, if a strip of iron metal is placed in a solution of copper sulfate,
copper ions deposit on the iron strip as copper metal, as the iron dissolves into solution
by the following reaction:
Fe + CuSO4 Cu + FeSO4
In comparing reactions to produce one molecule of hydrogen requires two atoms of
sodium but only one atom of magnesium, because sodium has a charge of +1, while the
magnesium ion has a charge of +2. This provides one basis for the concept of
equivalent weight. The equivalent weight of a cation is that weight which replaces 1.0 g
of hydrogen from aqueous solution. Another way to determine equivalent weight is the
molecular weight of a substance divided by its valence. Thus, the equivalent weight of
sodium is equal to its molecular weight, and the equivalent weight of magnesium
is half its molecular weight. Following Table shows the molecular weights and equivalent
weights for common compounds encountered in water treatment.
Some of the elements that form cations in aqueous solution belong to the following
groups:
Alkali metals (lithium, sodium, potassium, etc.)
Alkaline earth metals (magnesium, calcium, strontium, etc.)
Some transition metals (iron, manganese, zinc, etc.)
Some of the elements that form anions in aqueous solution belong to the following
groups:
Halogens (fluorine, chlorine, bromine, etc.)
Other nonmetals (oxygen, sulfur, selenium, etc.)
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Colloidal Systems:
Some types of matter can be dispersed in water even though not truly soluble.
Dispersion is accomplished by breaking down the material into extremely small particles,
slightly larger than ions and molecules.
Particles of this size, suspended in liquid, are called colloids The surface of almost all
matter (glass, steel, plastic, etc.) has a residue of electric charges. This can lead to the
development of high surface voltage, as demonstrated on a small scale by the discharge
of a spark of static electricity on a cold dry day and on a large scale by lightning. As
particles become smaller, the ratio of surface charge to mass increases exponentially.
Assume that a cube of sand measuring 1.0 mm on each side is reduced to colloidal
cubes of 100 nm (1 nm = 106 mm) on each side; this would produce 1012 colloidal
particles with a total surface 10 000 times larger than the original grain with a
correspondingly larger surface charge. It is this high surface charge that causes colloidal
particles to repel one another, thus maintaining stability of the dispersion.
On the other end of the scale is ammonia, which dissolves and ionizes to form a weak
base:
These are both equilibrium reactions, meaning that addition of more gas to the water
produces more acidic conditions and more basic conditions. On the other hand, addition
of acid would drive in acidic conditions equation to the left. Similarly, addition of base in
basic conditions equation would drive that reaction to the left.
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The ions in square brackets indicate the concentration of either calcium or carbonate in
mol/L. The solubility product is expressed in mol2/L2.
In a reaction where more than a single cation and anion are formed, the expression is
more involved, as with magnesium hydroxide:
Curve showing the balance of calcium ions versus carbonate ions in saturated CaCO3 solutions forms hyperbola
However, analysis of the precipitated floc shows the presence of sulfate in the solids,
indicating that some SO42 anions replaced OH anions in the lattice of the precipitate.
This affects the solubility of aluminum hydroxide.
A final factor affecting solubility of these slightly soluble compounds is the ionic strength
of the aqueous solution. The higher the concentration of ions in solution, the more
soluble is the precipitate.
This means that CaSO4, for example, is more soluble in seawater, containing about 30
000 mg/L NaCl, and in oilfield brines, containing up to 150 000 mg/L NaCl, than in
freshwater containing 100 mg/L dissolved solids. The solubility increase with ionic
strength is shown in Fig. below. The solubility product then is seen to be a useful
concept when used qualitatively, or developed empirically for a specific system.
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This equilibrium reaction can be expressed mathematically by the equation for the
equilibrium constant (K):
Calcium sulfate (gypsum) solubility increases with increasing sodium chloride concentration
Strong electrolytes, such as sodium chloride, completely ionize in freshwater, so that the
equilibrium constant is of no value in calculations involving this particular salt. However,
calculations involving weak electrolytes rely on the equilibrium constant to show the
distribution of the reacting materials and products both in their ionic and nonionized
forms. This provides data useful in selecting chemical processes for removal of various
contaminants from water. For example, the equilibrium constants for gases that ionize in
water, such as hydrogen sulfide and ammonia, make it possible to calculate the
optimum pH values for removal of these materials from water in their gaseous form.
Typical dissociation constants are shown in Table below.
Solid Reactants
There are two distinctive mechanisms by which materials dissolved in water react with
solids: adsorption and ion exchange.
Adsorption
Adsorption is the adhesion of a layer of molecules or colloidal particles to the surface of
a solid, which is usually porous. The gas mask is a common illustration of the use of this
process. The mask contains a canister of adsorbent material, usually activated carbon,
capable of removing and storing hazardous or toxic gases, so that the person wearing
the mask can safely breathe in a contaminated atmosphere.
In water systems, activated carbon removes organic molecules that cause taste and
odor problems. Another example is the adsorption of silica (SiO2), a negatively charged
colloid, on freshly precipitated magnesium hydroxide [Mg(OH)2].
Complexing Agents
A complex is a species formed by the association of two or more simpler species, each
capable of independent existence. When one of these species is a metal ion, the
resulting entity is known as a metal complex. Complexing agents are called ligands (or
sequestrants or chelants) that act as an electron donor in a complex reaction. The ligand
must have at least one pair of electrons to donate to the metal ion, forming a shared
electron pair bond (coordinate covalent bond).
A characteristic feature of such a complex is that the metal ion occupies a central
position in the matrix.
A ligand with one electron pair donor site is an undentate ligand. An example is
ammonia (NH3) as shown in Fig. below. The water molecule (H2O) is shown as a ligand.
A bidentate ligand has two electron pair donor sites, such as ethylenediamine
(NH2CH2CH2NH2).