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DESPIAGIA PITALOKA
FARHAN SUBAKTI
NADIA PUTRI
TP 2018/2019
CHAPTER I
PRELIMINARY
Interpretation
Principle of Spectrophotometer
1.Source of polycromatic light function as a source of polycromatic light with various lengths
of gewave.
2.The monochromator functions as a wavelength selector that is changing light that comes
from a polycromatic light source become light monokromatis.On the picture above is referred
to as disperser or spreader light. with the presence of dispersers only one type of light or light
with a single wavelength affecting the sample cell. In the picture on for only the green light
that passes through the exit.
Probsession or dispersion spread of light as shown in the picture.
2. Process
Dispersion light
3. Sample cells function as a place to place samples
-UV, VIS and UV
-VIS uses the cuvette as a sample place. Kuvet usually made of quartz or glass, but a quartz
cuvette made from silica has better quality. This is due to being made from 6 glass and plastic
can absorb UV so its use is only on spectro Visible light meter (VIS). Kuvet bias I am
rectangular
with a width of 1 cm.
-IR, for liquid and solid samples (in the form of paste) is usually applied to
two sodium chloride plates. For samples in the form of a solution, enter it in sodium chloride
cells. This cell will be solved to take it back the solution analyzed, if the sample is owned by
him at a little and the price expensive.
4. The detector functions to capture the light transmitted from the sample and
turn it into an electric current.
Kind of
-type of detector that is
Phot detectoro
(Photo detector), Photocell, for example CdS, Phototube, photo delivery
, Photo diodes,
Heat detector
5. Read out is a reading system that captures the amount of electrical signals
which derive from detector.
As for things
-things that must be considered in spectrofotometry is:
a.At the time of dilution the dilution device must be correct
-really clean without
presence of impurities
b.In the use of tools
-the tool must be correct
-really sterile
c.The amount of substance used must be in accordance with what has been determined
d.In the use of spect UV rofotometry, the sample must be clear and not cloudy
e.In the use of UV spectrophotometry
-vis, the sample must be colored.
Uptake can occur if the photons / radiation that hit the snippet have the same energy
with the energy needed to cause it to occur power change. If monochromatic light is passed
through a layer of solution
with thickness(db), then decreased intensity of light (dl)because it passes through layers
the solution is proportionaldirectly with radiation intensity.
concentration
species that absorb (c), and with the thickness of the solution layer (db)
How to use :
1. The polycromatic light source enters the monochromator (here the light spreads)
2. From the monochromator then goes out to the sample cell, in this sample cell occurs the
process of absorption of light by substances in the sample cell (where the incoming light is
brighter compared to light after exiting)
3. Then the light is captured by the detector and changes it
CHAPTER III
CONCLUSION
Through this practical activity, several techniques can be identified in the use of UV / Vis
spectrophotometers by measuring samples in various concentrations, finding the maximum
transmittance value, creating a standard curve and determining its concentration. The
spectrophotometer produces light from a spectrum with a certain wavelength and the
photometer is a measuring device for the intensity of the transmitted light or adsorbed. So a
spectrophotometer is used to measure energy relative if the energy is transmitted, reflected or
emitted as a function of wavelength.