Reference literature. (See: CHEM 2470 notes, Module 8 Textbook 6th ed., Chapters )

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Transcription:

September 17, 2018

Reference literature (See: CHEM 2470 notes, Module 8 Textbook 6th ed., Chapters 13-14 )

Reference.: https://slideplayer.com/slide/8354408/

Spectroscopy Usual Wavelength Type of Quantum Transition Gamma-ray emission 0.005 1.4 Å Nuclear X-ray absorption, emission, fluorescence, and diffraction 0.1 100 Å Inner electron Vacuum UV absorption 10-180 nm Bonding electrons UV-visible absorption, emission and fluorescence IR absorption and Raman scattering 180 780 nm Bonding electrons and Electrons in n transfer bonds 0.78 300 m Rotation/vibration of molecules Microwave absorption 0.75 3.75 mm Rotation of molecules Electron spin resonance Nuclear magnetic resonance 3 cm Spin of electrons in a magnetic field 0.6 10 m Spin of nuclei in a magnetic field

Absorbance is additive: A = bc A 1 M+N = A 1 M + A 1 N = 1 Mbc M + 1 Nbc N A 2 M+N = 2 Mbc M + 2 Nbc N 6

Instrumentation for spectroscopy

Instrumentation for Spectroscopy Most spectroscopic instruments are made up of five key components: Radiation source Wavelength selector to isolate a restricted wavelength region Sample container(s) Radiation detector or transducer to converts radiant energy to a measurable signal (usually electrical) Signal processor and readout

Examples of Continuum Radiation Sources: Deuterium Lamp D or H Gas 2 2 40V Electric Arc Filament Sealed Quartz Tube Electrode Deuterium Lamp D 2 + E elect D 2 * D + D + hν Based on electric excitation of D 2 at low pressure Good for ~200-500 nm; short intensity half-life (~1000 hr)

Examples of Continuum Radiation Sources: Xenon Lamp Good for the 250 nm - visible regions higher noise 15

Wavelength Selectors To restrict the wavelength to a narrow band that is absorbed or emitted by the analyte, in order to enhance the selectivity and sensitivity of the instrument. Ideally a wavelength selector should produce a single wavelength; in reality, it always produce a narrow band. Filters Monochromators

Wavelength selection: Monochromators Separating wavelengths continuously (scanning) from polychromatic light in time or space to allow only certain λ s to be selected and used. A monochromator typically consists of: Prisms or gratings Slits Lenses Mirrors Windows

Echellette-type grating (conventional) Light is reflected off the longer side of the blazes in the grating. i) grooved (blazed) with broad faces where diffraction occurs and narrow unused faces ii) high groove density (large number of grooves/mm) meaning d is small iii) most light diffracted into first order iv) low blaze angle (r) nl = d(sini + sinr)

Sample Holders The sample holders (known as cells or cuvettes) must: Not be reactive with the sample Be transparent to the wavelengths of in use Be readily cleaned for reuse Fit the specific instrument of interest

Detectors: Devices that convert light to electrical signal. Ideally, they should have: High and fast conversion yield (sensitivity) Good S/N Constant response over λ range of interest Signal proportional to light intensity Little or no signal in absence of light (dark current)

Photomultiplier tubes

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 10 6 10 7 electrons, and as such current is amplified and measured. Advantages: very sensitive to low intensity, very fast response. Disadvantages: need high voltage power supply; intense light damages at high power radiation

Silicon Photodiode Detectors Semiconductor material conducts current only under certain conditions Process: Solid-state detector; more reliable and robust. Sensitivity a little lower than that of PMTs - A reverse-biased pn junction silicon (190-1100 nm) or germanium (800-1700 nm) diode. - No current when there is no light due to the non-conducting depletion layer. - When light strikes, it produces electrons and holes in the depletion layer and thus produces a current that is proportional to radiant power.

Photodiode Arrays (PDAs) Consisting of a series (200-1000) of photodiodes each of which consists of a reversebiased pn junction, positioned side by side on a single silicon crystal. Process: - Each diode has a dedicated capacitor and is connected by a solid-state switch to a common output line. The switches are controlled by a shift register. - Initially, the capacitors are charged to a specific level. Solid-state detector; Measuring the entire wavelength range essentially simultaneously. - When photons penetrate the silicon, free electrical charge carriers are generated that discharge the capacitors. The capacitors are recharged at regular intervals that represent the measurement period for each scanning cycle. - The amount of charge needed to recharge the capacitors is proportional to the number of photons detected by each diode, which in turn is proportional to the light intensity.

Single vs. double beam UV-Vis absorption spectrophotometers uses a beam chopper to separate the reference beam from the sample beam. Single-Beam

Limitations to Beer s Law Chemical Deviations: (1) Real deviations due to high concentrations When c is too high (e.g., > 0.01 M), the distance between analyte molecules decreases to the extent that they change each other s charge distribution, modifying radiation is absorbed.

(2) Apparent deviations due to chemical reactions If the analyte associates, dissociates, or reacts with the solvent or other components in the solution, deviations from Beer s Law will occur due to the formation of molecules with different. Example: HIn = H + + In - 430 6.30x10 2 7.12x10 3 570 2.06x10 4 9.61x10 2 Apparent deviation since can be accounted for by chemical equilibrium 29

Quantitative method Method based on the formation of complexes with 4-(2-pyridylazo)resorcinol. The absorbance band yielded by the mixture is resolved by applying multilinear regression to the corrected, standardized spectrum of each metal ion as standard. Provides a linear determination range of 0.10-4.0 pg/ml for Ca and 0.15-2.5 pg/ml for Mg and can be applied to the analysis of various types of water. Based on the use of a diode array detector.

Ca 2+ + nligand Ca Ligand n ε of complexes formed between metal ions and 4-(2-pyridylazo)resorcinol (PAR) are on the order of 10 4 Lmol -1 cm -1 H

Method: 1) For background subtraction: Measure 3 spectra of PAR at 6 x 10-4 M, average and use as PAR spectrum to subtract from other spectra. Range: 470-650 nm. 2) Calibration curves: 0.10-4.0 pg/ml for Ca and 0.15-2.5 pg/ml for Mg, with 6 x 10-4 M PAR. Spectra were recorded and subtracted with 1) and calibration curves were obtained at each l (J). 3) Unknowns: Spectra were recorded and subtracted for PAR with 1). Under the assumption that Beer s law is obeyed and additive, a matrix corresponding to N absorbing components at J wavelengths was created.

Maxima: 490 nm (Mg, i = 1) and 502 nm (Ca, i = 2). Wavelength range for multi-regression: 470-650 nm (j = 490, 491, 492. 502).

N A j = ij bc i + k 0 i=1 A j : absorbance of the mixture at wavelength j ij : molar absorptivity of species i at wavelength j c i : concentration of species i The ij values were obtained from the standard spectra of the i components k 0 : experimental error term (residual)

The matrix was solved by using a multilinear regression treatment based on determining the concentrations of the i components of the unknown sample with a minimum experimental error by matrix calculus.

Conclusions on UV-vis section Relatively inexpensive Covers a broad range of analytes (chemical modification may be necessary) Not as sensitive as fluorescence (by 100-1000 x) Often used in preliminary analysis of samples

Questions 1. The absorbance of a solution is 0.37. If the transmittance value of the blank sample (T 0 ) is 97%, what is the transmittance T of the solution? 2. In analytical chemistry, a spectrophotometer is mainly used : a) To measure the concentration of a mixture of unknown compounds b) To measure the concentration of a known light absorbing compound. c) To identify compounds by their retention time. d) To determine the extinction coefficients of unknown compounds. e) To study the relationships between absorption bands and structure.