spectrophotometry lecture. interaction of radiation and matter

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Spectrophotomet ry Lecture

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Page 1: Spectrophotometry Lecture. Interaction of Radiation and Matter

SpectrophotometryLecture

Page 2: Spectrophotometry Lecture. Interaction of Radiation and Matter
Page 3: Spectrophotometry Lecture. Interaction of Radiation and Matter

Interaction of Radiation and Matter

Page 4: Spectrophotometry Lecture. Interaction of Radiation and Matter
Page 5: Spectrophotometry Lecture. Interaction of Radiation and Matter
Page 6: Spectrophotometry Lecture. Interaction of Radiation and Matter

Absorption and Fluorescence

Page 7: Spectrophotometry Lecture. Interaction of Radiation and Matter

Terms

Page 8: Spectrophotometry Lecture. Interaction of Radiation and Matter

Interaction of Light with Matter

Page 9: Spectrophotometry Lecture. Interaction of Radiation and Matter
Page 10: Spectrophotometry Lecture. Interaction of Radiation and Matter

Molecules Absorption Wavelengths

Page 11: Spectrophotometry Lecture. Interaction of Radiation and Matter

Spectrophotometry

Although a number of different types of spectrophotometers exist all have one thing in common. Utilize light energy to detect molecules in a solution Light energy is reported to the user as wavelengths in

nanometers (nm) Different spec’s utilize wavelengths that fall into different

ranges. Visible (VIS) 350-700 nm Ultraviolet (UV) 200-350 nm

Page 12: Spectrophotometry Lecture. Interaction of Radiation and Matter

Absorption Spectrophotometer

Page 13: Spectrophotometry Lecture. Interaction of Radiation and Matter

Spectrophotometer

Page 14: Spectrophotometry Lecture. Interaction of Radiation and Matter

Spectrophotometer

spectrophotometer measures intensity of a light beam after it is directed through and emerges from a solution Ex: solution of copper sulfate (CuSO4) absorbs light The red part of spectrum has been almost complete

absorbed by CuSO4 and blue light has been transmitted

Gain greater sensitivity by directing red light through the solution because CuSO4 absorbs strongest at the red end of the visible spectrum

But to do this, we have to isolate the red wavelengths

Page 15: Spectrophotometry Lecture. Interaction of Radiation and Matter

Spectrum of visible light How do you isolate red wavelengths of light?

In a spectrophotometer, a light source gives off white light which strikes a prism, separating light into its component wavelengths:

Red wavelengths pass through CuSO4 solution and measure amount of red light absorbed

Colored compounds absorb light differently depending on the l of incident light

l = Wavelength, nm=nanometers

Page 16: Spectrophotometry Lecture. Interaction of Radiation and Matter

Design of Spectrophotometer

THE BLANK In order to effectively use a spectrophotometer we must first

zero the machine Blank contains everything except compound of interest which

absorbs light. By zeroing machine using "the blank," any measured absorbance is due to the presence of solute of interest

ABSORPTION SPECTRUM Different compounds having dissimilar atomic and molecular

interactions have characteristic absorption phenomena and absorption spectra which differ

The point (wavelength) at which any given solute exhibits maximum absorption of light (the peaks on the curves on the figure below) is defined as that compounds particular lmax

Page 17: Spectrophotometry Lecture. Interaction of Radiation and Matter

Design of Spectrophotometer

Page 18: Spectrophotometry Lecture. Interaction of Radiation and Matter

Electromagnetic Spectrum

Page 19: Spectrophotometry Lecture. Interaction of Radiation and Matter

How is Does a Spectrophotometer Work? Amount of a particular molecule of interest

is measured according to amount of light that is absorbedAbsorbance data is compared to a standard

of a known concentration to determine the concentration of the unknown.

Page 20: Spectrophotometry Lecture. Interaction of Radiation and Matter

How is Does a Spectrophotometer Work? All spec’s share

following common features: Lamp

i.e. tungsten or deuterium

Prism or grating Sample holder Display

Page 21: Spectrophotometry Lecture. Interaction of Radiation and Matter

Absorption Spectrophotometer

Page 22: Spectrophotometry Lecture. Interaction of Radiation and Matter

Absorption Curve

Page 23: Spectrophotometry Lecture. Interaction of Radiation and Matter

Background, B

Page 24: Spectrophotometry Lecture. Interaction of Radiation and Matter

Detection Limit DL or LOD

Page 25: Spectrophotometry Lecture. Interaction of Radiation and Matter

Dynamic or linear range

Page 26: Spectrophotometry Lecture. Interaction of Radiation and Matter

Sensitivity

Page 27: Spectrophotometry Lecture. Interaction of Radiation and Matter

Calibration Curve

Page 28: Spectrophotometry Lecture. Interaction of Radiation and Matter

Calibration Curve Procedures

Page 29: Spectrophotometry Lecture. Interaction of Radiation and Matter

Calibration Curve Plot

Page 30: Spectrophotometry Lecture. Interaction of Radiation and Matter

Example Nitrite Analysis

Page 31: Spectrophotometry Lecture. Interaction of Radiation and Matter

Results

Page 32: Spectrophotometry Lecture. Interaction of Radiation and Matter

Plot of Results

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Best Fit Line

Page 34: Spectrophotometry Lecture. Interaction of Radiation and Matter

How are Concentrations Obtained Using a Spec? More molec…more to absorb light

Note peaks of absorption curves Lambdamax

Wavelength at which a molecule absorbs the most light

Proteins, like other molecules, interact with certain wavelengths of light Proteins absorption spectrum can

be determined by measuring proteins light absorbance at different wavelengths.

Determine the lambdamax for protein

Page 35: Spectrophotometry Lecture. Interaction of Radiation and Matter

How are Concentrations Obtained Using a Spec? Most proteins are colorless

Light in visible range will not workLight in UV range will work for a colorless

solution ~280 nm Does NOT distinguish between different protein

types in a solution

Page 36: Spectrophotometry Lecture. Interaction of Radiation and Matter

Using Bradford Reagent

Way to colorize proteins and use white light spectroscopy Solution changes from

brown to blue when proteins present.

Degree of “blueness” of Bradford-protein mixture can be used to determine concentration of protein in a solution

Page 37: Spectrophotometry Lecture. Interaction of Radiation and Matter

How are Concentrations Obtained Using a Spec? Calculating protein

concentration in an unknown sample Known standards are

mixed with Bradford reagent and their absorbance values are determined

Standard curve generated. known absorbance values

can be plotted and concentrations determined

Page 38: Spectrophotometry Lecture. Interaction of Radiation and Matter

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