1. Satish Pradhan Dnyanasadhana College, Thane. Department of Chemistry S
Satish Pradhan Dnyanasadhana College, Thane. Department of Chemistry S.Y.B.Sc. Analytical Chemistry Paper-I Sem-IV UV-Visible spectroscopy Dr.G.R.Bhagure

2. 3.1.1 Errors in Chemical analysis: Types of errors-Determinate and Indeterminate errors-Constant and Proportionate errors, Absolute and Relative error-Minimization of errors
3.1.2 Measures of central tendency and dispersion :
Measures of central tendency-Mean, Median, Mode.
Measures of dispersion- Deviation, Average deviation, Relative average deviation ,Range , Standard deviation, Variance, Correlation coefficient and Relative standard deviation (Numerical problems expected)
3.1.3Performance Characteristics of an Analytical method: Accuracy, Precision, Sensitivity, Specificity, Selectivity, Robustness, Ruggedness, Linearity range, Limit of quantification, Limit of Detection, Signal to Noise ratio.
3.2 TITRIMETRIC ANALYSIS-IV (3L)
Precipitation titrations
Argentimetric titrations, Construction of titration curves, Volhard”s method, Mohr’s method, Adsorption indicators- theory and applications

3. WELCOME S.Y.B.Sc. Analytical Chemistry

4. Spectroscopy is branch of Analytical Chemistry which deals with study of interaction of electromagnetic radiation with matter.
In Ultra Violet and Visible Spectroscopy absorption of light is measured in the wavelength region from 200 nm to 800 nm.

5. The instrument used in Ultra violet and visible region (from 200 nm to 800 nm) is called as spectrophotometer.
The instrument used for measurement of absorption of light in visible region (from 400 nm to 800 nm) is called as colorimeter or photometer.

6. Quantum theory of Radiation
Black Body
White Body

7. Energy for Atom and Molecule
Electronic Energy
Electronic Energy
Atom
Atom
Rotational Energy
Vibrational Energy

8. CH3----------------- CH3
Rotational Energy
CH CH3
Motion of molecule from the centre of joining the nuclei

9. Bond length 154 pm, Stretching
Vibrational Energy
Bond length 154 pm,
Stretching
10 pm.
For a C-C bond with a bond length of 154 pm, the variation is about 10 pm.

10. C C C 4o Bending 10 pm Vibrational Energy
For C-C-C bond angle a change of 4o is typical. This moves a carbon atom about 10 pm.

11. Regions of Absorption
U.V. nm
Visible nm

12. Laws of Absorption Lamberts Law: (1760)
When monochromatic light is allow to pass trough a transparent medium, the rate of decrease of intensity of incident light with the thickness of the absorbing medium is directly proportional to intensity of incident light. OR
Equal fractions of the incident radiation are absorbed by successive layers of equal thickness containing the same no .of absorbing species

13. Laws of Absorption Beers Law: (1760)
When monochromatic light is allow to pass through a solution, the rate of decrease of intensity of incident light with the concentration of solution is directly proportional to intensity of incident light. OR
Equal fractions of the incident radiation are absorbed by successive layers of solution containing the same no .of absorbing species

14. I2 Io As per lamberts law Layer –II
Radiation absorbed is directly proportional to distance covered by light
 L  I1
 L
Layer –I
Layer –II I2 Io
As per lamberts law

15. Deviation from Beer-Lambert’s Law
According to Beers Lamberts Law
A= € x lx C OR A= log10Io/It
Where:
A= Absorbance
€ = Molar absorbance
l= Path length in cm.
C= Concentration in Mole/L
According to the above equation
Absorbance is directly proportional to concentration

16. A is Directly proportional to concentration
Absorbance--
Concentration 

17. Positive Deviation Beers Lamberts Law verified Absorbance--
Negative Devitation
Concentration 

18. Deviation from Beer’s Lamberts Law
TYPES OF DEVIATION
Real Deviation
Chemical Deviation
Instrumental Deviation

19. 1) Real Deviation:- Concentration should be below 0.01M
At higher concentration average distance between molecule decreases which affect in absorbance.
Molar absorptivity changes because at higher concentration refractive index of solution changes
High Concentrated
Low concentrated

20. 2) Chemical Deviation:-
This deviation occurs when solute present in solution undergoes association, dissociation or ionization.
Association: Diluting or concentrating the solution of Benzyl alcohol in chloroform undergoes polymerization.
4C6H5CH2OH---->(C6H5CH2OH)4
Dissociation:-Ex. K2Cr207
Cr H20 2HCrO4 2H+ +2CrO42-
(Orange) (Yellow)

22. 3)Instrumentatal Deviation
The law is valid If light used is strictly monochromatic. If not deviation may occur.
Deviation may occur if width of slit is not proper which may allow undesired radiation to pass through it. 22
MCL
PCL

23. INSTRUMENT
Colorimeter OR
Photometer nm
Spectrophotometer
nm.

24. INSTRUMENTATIONS
The various components of instruments and type of instruments used is called as Instrumentation.
Instrument used in visible region (400 to 800 nm) is called as colorimeter or photometer
Instrument used in Ultra violet & visible region (200 to 800 nm) is called as Spectrophotometer.
The basic component of the instruments are
Radiation Source (Tungsten Filament lamp/ hydrogen or deuterium lamp)
Wave length selector( Filter/ monochromator)
Sample cell
Detector

25. INSTRUMENT
Colorimeter OR
Photometer nm
Spectrophotometer
nm.

26. PHOTO CELL
DETECTOR
Detectors:-
PHOTO
MULTIPLIER
TUBE
PHOTOTUBES

27. Semiconductor Selenium B
PHOTOCELL DETECTOR
(--) D D G C E- G B A +
Iron plate A
Semiconductor Selenium B
Thin layer of silver C

28. Construction: It consists of Iron plate A on which a thin layer of a semiconductor like Selenium B is deposited. The layer is covered by very thin layer of silver C that acts as collector electrode. A ring D can hold the silver plate in its place.
Working:-This cell operates without battery. When the transmitted beam of light passes through thin film of silver metal to selenium layer, electrons released from semiconductor surface .These electrons pass through a hypothetical barrier layer in between silver and selenium layer and are collected by silver electrode.
Thus under the action of light a cell is formed with iron plate as positive electrode
Metal ring as negative electrode. The current flow is detected in galvanometer. This current is directly proportional to absorbance.

29. PHOTO TUBE DETECTOR - AMPLIFIER RECORDER Collector Anode (+)
Photo Cathode (-)
Collector Anode (+) -
AMPLIFIER RECORDER

30. PHOTOMULTIPLIER TUBE DETECTOR

31. Single Beam Photometer
Radiation Source Collimating Lens Filter Sample Cell Photocell Read Out Device

32. Working of Single Beam photometer
Quantitative analysis can be performed by calibration curve method.
Instrument is adjusted to 0 absorbance or 100% transmittance by Using Blank Solvent at a particular wavelength.
The absorbance of sample solution as well as standard solution are measured.

33. Distinguish Between Photometer and Spectrophotometer
Radiation source is Tungsten filament lamp.
Absorbance of light is measured in the wavelength nm.( Visible region)
Filters are used to select monochromatic light.
Sample cells made from glass.
Detectors used are photocell or photoemmisive tube.
Absorbance of coloured solution is measured
SPECTROPHOTOMETER.
Radiation source is Hydrogen or deuterium lamp.
Absorbance of light is measured in the wavelength nm. (U.V.& Visible region)
Prism or Gratings are used to select monochromatic light.
Sample cells made from quartz.
Detectors used are photomultiplier tube.
Absorbance of coloured as well as colorless solution can be measured

34. LIGHT DISPERSING DEVICES MONOCHROMATORS SPECTROPHOTOMETERS
FILTERS
(COLORIMETERS )
MONOCHROMATORS SPECTROPHOTOMETERS

35. Filter: A filter transmits the monochromatic beam of light and absorbs other light
Polychromatic light
Monochromatic light

36. PRISM MONOCHROMATOR FOCUSING LENS COLLIMATING LENS PRISM ENTRANCE SLIT
LAMBDA-1
LAMBDA-2
PRISM
ENTRANCE SLIT
EXIT SLIT
PRISM MONOCHROMATOR

37. GRATING MONOCHROMATOR
MAGINIFIED VIEW
ENLARGED VIEW
GRATING MONOCHROMATOR

38. Applications of U.V. & Visible Spectroscopy
Qualitative Analysis
Identification of Structural Groups in Molecules.
Spectroscopic analysis of a substance is carried out using radiation of a particular wavelength this wave length is called as Lambda Max. The Constituent groups in a molecule absorbed to their characteristic wavelengths.
It is possible to determine a particular group in a molecule by determining its Lambda Max. Lambda Max values of important groups are given in following table.

39. A B S O N C E Wavelength --- 200 300 400 500 600 700 800
The Wavelength at which absorbance of highly
concentrated solution is maximum is called as Lambda max. A B S O N C E
Lambda Max
Wavelength ---

40. Example Functional Groups Lambda Max ( nm) Solvents Acetic Acid --COOH
208
Ethyl Alcohol
Acetyl Chloride
--COCl
220
Hexane
Acetamide
--CONH2
178
Nitromethane
--NO2
201
Methyl Alcohol
Azomethane
--N=N--
338
Acetaldehyde
>C=O
290
Acetone
189

41. Applications of U.V. & Visible Spectroscopy
Quantitative Analysis By Calibration Curve Method

42. Other Applications
UV and visible spectroscopy can be used up to concentrations up to and some times up to 10-7 M.
Qualitative analysis can be performed because each absorbing species absorb at different wave length.
It used in water and air pollution studies.
It is also used to study the complexes and in the determination of complex.
It is used in industry to monitor various process controls.
It is also used to study to distinguish between cis-and trans isomerism. C- is isomer absorbs at shorter wave length and trans isomer absorb at longer wave length.

43. Questions? Please

44. All the best