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Absorption Spectroscopy Introduction A.) Absorption : electromagnetic (light) energy is transferred to atoms, ions, or molecules in the sample. Results in a transition to a higher energy state. - Transition can be change in electronic levels, vibrations, rotations, translation, etc. - Concentrate on Molecular Spectrum in UV/Vis (electronic transition) - Power (P) : energy of a beam that reaches a given area per second E o E 1 h Energy required of photon to give this transition: h E = E 1 - E o (excited state) (ground state)
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Absorption Spectroscopy

Jan 04, 2016

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Mark Wood

Absorption Spectroscopy. Introduction A.) Absorption : electromagnetic (light) energy is transferred to atoms, ions, or molecules in the sample. Results in a transition to a higher energy state. Transition can be change in electronic levels, vibrations, rotations, translation, etc. - PowerPoint PPT Presentation
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Page 1: Absorption Spectroscopy

Absorption Spectroscopy Introduction

A.) Absorption: electromagnetic (light) energy is transferred to atoms, ions, or molecules in the sample. Results in a transition to a higher energy state.

- Transition can be change in electronic levels, vibrations, rotations, translation, etc.

- Concentrate on Molecular Spectrum in UV/Vis (electronic transition)

- Power (P): energy of a beam that reaches a given area per second

- Intensity (I): power per unit solid angle

- P and I related to amplitude2

Eo

E1h Energy required of photon to give this transition:

hE= E1 - Eo

(excited state)

(ground state)

Page 2: Absorption Spectroscopy

B.) Terms:

1.) Beer’s Law: A = bc

The amount of light absorbed (A) by a sample is dependent on the path length (b), concentration of the sample (c) and a proportionality constant (– molar absorptivity)

Amount of light absorbed is dependent on frequency () or wavelength ()

c

Absorbance is directly proportional to concentration Fe+2

Increasing Fe+2 concentration

Page 3: Absorption Spectroscopy

B.) Terms:

1.) Beer’s Law: A = bc

Transmittance (T) = P/Po %Transmittance = %T = 100T

Absorbance (A) = log10 Po/P

No light absorbed- % transmittance is 100% absorbance is 0

All light absorbed- % transmittance is 0% absorbance is infinite

Page 4: Absorption Spectroscopy

Relationship Described in Terms of Beer’s Law

A = Absorbance = bc = -log(%T/100)

= molar absorptivity: constant for a compound at a given frequency () or wavelength () units of L mol-1 cm-1

b = path length: cell distance in cm

c = concentration: sample concentration in moles per liter.

Therefore, by measuring absorbance or percent transmittance at a given frequency can get information related to the amount of sample (c) present with an identified and .

Note: law does not hold at high concentrations, when A > 1

Page 5: Absorption Spectroscopy

Example 4: A solution that was 3.78x10-3 M in X had a transmittance of 0.212 when measured in a 2.00-cm cell. What concentration of X would be required for the transmittance to be increased by a factor of 3 when a 2.00-cm cell was used?

Page 6: Absorption Spectroscopy

C.) Components of an Instrument for UV/Vis Absorbance Measurements:

1.) Basic Design:

Hitachi Instruments U-3010

Light Source, selector, Sample cell holder, Detector (amplifier, recorder)

Page 7: Absorption Spectroscopy

a) Desired Properties of Components of UV/Vis:

Light Source Selector Creates Proper Narrow Band pass:Stable: Selects Desired Constant P Large Light Throughput:

Good Precision Increase PIntense:

Increase PEasier to See Absorbance

Sample Cell Holder DetectorFixed Geometry: Stable

Constant b Sensitive to of InterestTransmits of Interest:

Increase P

Page 8: Absorption Spectroscopy

b) Light Sources UV/Vis (~ 200 – 800 nm):

1. Deuterium & Hydrogen Lamps (UV range)- continuous source, broad range of frequencies- based on electric excitation of H2 or D2 at Low pressure

40V Electric Arc

Electrode

Filament

D or H Gas2 2

Sealed Quartz Tube

In presence of arc, some of the electrical energy is absorbed by D2 (or H2) which results in the disassociation of the gas and release of light

D2 + Eelect D*2 D’ + D’’ + h(light produced)

Excited state

Page 9: Absorption Spectroscopy

- h will vary continuously from ~ 160nm up to 375nm (UV range) due to different frequencies going into D’ and D’’

- need to make cell from quartz since glass absorbs light at ≤ 350 nm

- cost ~ $350-$500

Intensity Spectrum Of Deuterium Arc Lamp

Page 10: Absorption Spectroscopy

2. Tungsten Filament Lamp (Vis – Near IR)- continuous source, broad range of frequencies- based on black body radiation:

heat solid filament to glowing, light emitted will be characteristic of temperature more than nature of solid filament

Low pressure (vacuum)

Tungsten Filament

Temperature Dependence of

Page 11: Absorption Spectroscopy

2. Tungsten Filament Lamp (Vis – Near IR)- max 1/T

Typical Tungsten lamp T ~ 2870K range: 350 – 2500 nm need high temperatures to get high light intensity and low max

- cost ~ $10-15

Page 12: Absorption Spectroscopy

3. Xenon Arc Lamps (UV – Vis Range)- Continuous source, broad range of frequencies

range: 250 – 600 nm- works by passage of current through Xe, causes thermal excitation

Blackbody emission- Gives Very intense radiation over frequency range.

developed for search lights during WWII - problems: higher heat, more stray light, higher cost, shorter lifetimes

Page 13: Absorption Spectroscopy

b) Wavelength Selectors:

1. Monochromator- separates frequencies () from polychromatic light.- allows only certain ’s to be selected and used.

i.) Dispersing Monochromator:

a) Prism: based on refraction of light and fact that different ’s have different values of refraction index (i) in a medium.

Page 14: Absorption Spectroscopy

Dispersion Curve: change in i as a function of

Normally want to work in areas of normal dispersions for prisms. Anomalous dispersion occurs near where substance itself absorbs light.

Page 15: Absorption Spectroscopy

1sin1sin2Recall Snell’s Law of Refraction

Also, remember that no refraction occurs if light at normal or = 0

So, light must hit prism at an angle.

Most common is a 60o prism (glass or quartz).

Page 16: Absorption Spectroscopy

ii.) Grating Monochromator: based on diffraction of light (constructive and deconstructive interference)

a) Transmission Grating: groves or slits placed on a transparent material. Same as earlier example shown in diffraction discussion

Order of Interference (n): n = d sin

Different ’s will have constructive interference at different points.

Can select desired by letting light at different points into instrument.

X

Y

n =0

n =1

n =1

n =2

Page 17: Absorption Spectroscopy

b) Reflection Grating: most commonly used- grooved surface with reflective coating (Al, Au, Pt)

Now, spacing of slits (d) is distance from one groove to next.Typically have 300-2000 grooves/mm.

Constructive and deconstructive interference occurs because light travels different distances when reflected from each grating

Angle at which constructive interference occurs is now given by:

n = d(sin i + sin r)

n = d(sin i + sin r)

Page 18: Absorption Spectroscopy

Example 5: A monochromator was equipped with an echellete grating of 2500 blazes per millimeter, where 2.0 cm of the grating was illuminated. At approximately 430 nm, what minimum wavelength difference could in theory be completely resolved by the instrument?

Page 19: Absorption Spectroscopy

iii.) Two Types of Monochromators:

a) Czerney-Turner Grating:

Important Components:i) Entrance slitii) Collimating lens or mirror – makes radiation parallel before hitting

dispersing elementiii) Grating or Prismiv) Focusing Lens or mirror – to focus light of desired on exit slit.

Page 20: Absorption Spectroscopy

iii.) Two Types of Monochromators:

b) Bunsen Prism:

Important Components:i) Entrance slitii) Collimating lens or mirror – makes radiation parallel before hitting

dispersing elementiii) Grating or Prismiv) Focusing Lens or mirror – to focus light of desired on exit slit.

Page 21: Absorption Spectroscopy

iv.) Comparison of Gratings vs. Prisms:

– increase size of either prism or grating will give better dispersion.– stray light can be removed with filters.– glass absorbs light ≤ 350 nm

Type of Dispersion Size Stray Light range of use

Grating uniform dispersion vs. smaller Higher stray light unlimited

Prism shorter better separated

larger Less of problem Limited( ≤ 350 nm)

Page 22: Absorption Spectroscopy

v.) Slits in the Monochromator:

- need to be carefully made, since they control the range of ’s emerging from the monochromator.

- typical slit widths are 0.01 – 2 mm are often adjustable.

a) Band pass of the monochromator: range of ’s transmitted at the half-height of transmitted light band.

Typical band pass : 20nm -0.5 nm for UV-vis instruments.

- decrease slit size decrease band pass (good).- less undesired ’s, but less intensity (bad).

Page 23: Absorption Spectroscopy

Two ’s can be resolved by the monochromator if they differ by 2 or more times the band pass.

- resolution is directly related to slit size.

Page 24: Absorption Spectroscopy

Effective bandwidth for two types of filters and the result of combining filters.

Page 25: Absorption Spectroscopy

2) Interference Filters- made up of thin layers of metal and dielectric (eq. CaF2) material sandwiched between glass plates- dielectric material is of uniform, known thickness.- metal acts as partial mirror

Page 26: Absorption Spectroscopy

As light enters, some goes through but some is reflected. The distance the light travels before it exits generates constructive and destructive interference on the other side of the filter.

’s transmitted through filter:

N = 2d

– refractive indexd – thickness of dielectricN – integer - wavelength

Band pass can be 1-20nm. (narrow), but filter is fixed at given value as much intensity is lost due to reflection

2) Interference Filters

Page 27: Absorption Spectroscopy

vi.) Sample Cell:

- Must be transparent at used. quartz or fused silica for UV (< 350 nm) glass or plastic for visible

- best if flat cells, with matched sample and reference cells.- many automated instruments have flow-through cells with temperature control.

vii.) Detectors:

a) earliest detectors were the eye or film. now use devices that convert light to electrical signal

b) for good detector want: high sensitivity good signal to noise ratio constant response over range of interest signal light intensity fast response little or no signal in absence of light (dark current)

Page 28: Absorption Spectroscopy

c) Many Types of Available Detectors for UV/VIS

1) photovoltaic cell (Barrier-Layer Cell)

Process:

light of sufficiently high energy passes through the thin transparent silver layer and hits selenium causing electrons to be released which move across barrier toward silver layer (electropositive) and collected at iron layer to neutralize selenium layer.

- Current produced is proportional to photons hitting surface- Maximum response at 550 nm (10% at 350-750 nm ~ same as human eye).

Advantage: cheap, rugged, no external power source, good for portable instruments.

Disadvantage: not very sensitive, shows fatigue (decrease in response with continued illumination), difficult to amplify signal-small resistance (Ohm’s law: I=(V/R)).

Page 29: Absorption Spectroscopy

2) Vacuum Phototube

(Photoemission material)

Process:- photoemission material (Cs2O) ejects an e- when “hit” with a photon (photoelectric effect).- potential of 90V across cathode(-) and anode(+). As light “hits” cathode, e- are emitted from cathode and attracted to anode. Produces current that can be measured.- current number of photons.- smaller current then photovoltaic cell, but can be amplified because of larger resistance.- 90V difference sufficient to collect all e- produced (working at saturation).- various photoemission material (sensitive to certain photon ’s)

Page 30: Absorption Spectroscopy

Process (cont.):- various photoemission material (sensitive to certain photon ’s)

- common to use phototubes in UV-Vis instruments one tube for UV & most visible region, second tube for red end of spectrum. some phototubes have “flat” regions throughout entire range (ex.128 Ga/As composite). sometimes gas is present in tube. As e- collide with gas, more e- and ions produce

results in an increase in current.

Advantages: sensitive, signal easily amplified.Disadvantages: some dark current (from thermal e- emission & natural decay of 40K in glass

housing

2) Vacuum Phototube

Page 31: Absorption Spectroscopy

3) Photomultiplier tube (PMT)

Dynodes – all covered with photoemissive material

Process: a) light hits cathode and e- emitted. b) an emitted e- is attracted to electrode #1 (dynode 1), which is 90V more positive. Causes several more e- to be emitted. c) these e- are attracted to dynode 2, which is 90V more positive then dynode 1, emitting more e-. d) process continues until e- are collected at anode after amplification at 9 dynodes. e) overall voltage between anode and cathode is 900V. f) one photon produces 106 – 107 electrons. g) current is amplified and measured

Advantages: very sensitive to low intensity, very fast response.Disadvantages: need high voltage power supply, intense light damages

Page 32: Absorption Spectroscopy

Reverse-bias: no current flows

Semiconductor material – conducts current only under certain conditions

free electrons inside the N-type material need some extra energy to overcome the repulsion of the P-type's acceptor atoms.

- Light shining on the silicon diode provides the energy needed for the electrons to travel into the P region.- Flow of current is related to intensity of light.

4) Silicon Diode or Photodiode detectors

Page 33: Absorption Spectroscopy

4) Silicon Diode or Photodiode detectors

- Not very sensitive, but useful in Vidicon Tubes- Vidicon tubes can be used for 1 & 2 dimensional detection

Detect all the ’s along the focal plane of an instrument

A vidicon tube contains many silicon diodes each insulated from each other (~ 8m apart). The e- gun or light source sweeps the P-region and charges the diodes. (Television)

Page 34: Absorption Spectroscopy

vii.) Single and Double Beam Instruments:

- To determine absorbance both Po and P must be measured.

- depends on: intensity of source slit width & of monochromator reflectance of the cell sensitivity of the detector

Absorbance (A) = log10 Po/P

Page 35: Absorption Spectroscopy

Process for a Single Beam Spectrometer:

a) Po is measured with solvent in the cell

b) P, blank everything except compound to be analyzed- spectrophotometer is adjusted to read 100%T or 0% A.- 0%T or A is set by blocking the light beam (P=0)- settings may change over a period of minutes (drift)

change in light source intensity

- settings are wavelength dependent

Spectronic 20

Schematic of Spectronic 20

Page 36: Absorption Spectroscopy

- Single beam spectrophotometer (340-625nm) other phototube goes to 950

nm (20 nm band pass)- Reference phototube electronically adjusts for changes in source intensity- The control turns the grating.- The 0%T adjust sets the meter to 0%T when the occluder blocks the light beam.- The 100% T adjusts moves a V-shaped slot into or out of the light beam so the meter reads 100%T

Advantages: cheap, rugged.Disadvantages: must readjust 100%T at every and periodically check for drift, cell is round so path length can vary if don’t have cell aligned the same each time

Page 37: Absorption Spectroscopy

Double Beam Spectrometer Decrease/Eliminates Single Beam Problems

Schematic of Hitachi 100-60

Selector mirror or beam chopper: mirrors which rotate at 60 cps, reflecting the light alternatively to the reference and sample cells

All light is combined and goes to a single PMT. Output of PMT is 60 cps square wave. Po and P are measured alternatively at a rate of 60 times per second.

Advantages: scanning, little drift – only one PMT.Disadvantages: more complex and expensive