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announcements and reminders
Homework #2 due Wednesday September 27 problems: chapter 7(15(a,c,f and g) , 19 and 22) chapter 8(4,5,7 and 8) last lecture: optical instruments intro atomic spectroscopy today’s lecture: atomic spectroscopy and start 1st inst: AAS
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Effect of Temperature Boltzmann Equation Example 8-2:
Ratio of Na atoms in the 3p excited state at K (Acetylene/Air) = Change in number of excited atoms for 10 K = 4%
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Band and Continuum Spectra
Band spectra – the additional vibrational and rotation energy levels of simple molecules (e.g., CaOH) result in broad (a few nm) spectral features Continuum Spectra – particulate matter within flame acts as a source of black body radiation
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Sample introduction Nebulization Electrothermal Vaporizer
sample is converted into a mist of finely divided droplets (aerosol) Electrothermal Vaporizer sample is vaporized and atomized within a closed tube that is electrically heated at temperatures up to 3000 K (page 203)
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Chemical conversion convert sample into a volatile molecular species that is more efficiently atomized. hydride generation (page 203) As-cmpds + NaBH4 → AsH3 cold vapor AAS Hg-cmpds and ions + SnCl2 → Hg0 US EPA Method 1631
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Solid Samples Electrothermal Ablation
sample is vaporized and atomized within a closed tube that is electrically heated at temperatures up to 3000 K (page 203) Ablation high energy discharge (electrical spark or arc; laser pulse) causes a plume of particulate and vaporized matter to be ejected from a solid surface.
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Direct Sample Insertion
Glow Discharge low pressure plasma in contact with the sample sputters the sample atoms (~0.1mg/min) Direct Sample Insertion self evident
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AAS Flame AAS: 1% precision possible (2-3% typical)
Useful for ~60 metals and metalloids Detection limits 1-20 ppb typical, depends on element Linear Dynamic Range: ~one order of magnitude Matrix effects: significant ~$30,000
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flame processes Oxidation: atoms metal oxides
(secondary combustion zone; yellow) Ionization: neutral atoms ions (interzonal region; measurement zone) Excitation - atom is thermally excited into a higher energy state Dissociation: molecules atoms (primary combustion zone; blue) Volatilization: salt particles gaseous molecules Desolvation: spray salt particles Relative importance of these processes depends upon: element flame temperature Hydrogen-Air C GC detectors Acetylene-Air C Best for non-refractory elements Acetylene-N2O C Best for refractory elements
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electrothermal AAS sample is vaporized and atomized within a closed tube that is electrically heated to 3000 K add-on to flame AAS Precision: 5-10% Matrix effects: severe Sample required: L Detection limits: ppb Better because holds atoms in light beam longer
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electrothermal process
Drying- removes solvent eg, 125C for 20 s Charring (Ashing) – destroy organic matter smoke cause strong signal (not related to concentration) eg., 1400 C for 60 s Atomize - rapidly vaporize sample and break it down to atoms rapid heating to C yields a transient signal (<1 second)
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Chemical conversion convert sample into a volatile molecular species that is more efficiently atomized e.g., hydride generation As-cmpds + NaBH4 ➔ AsH3 continuous signal (although the magnitude and temporal dependence will depend upon the reaction kinetics)
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hollow cathode lamp emits sharp atomic lines characteristic of the element from which the cathode is made simplicity of HCL spectra means that a low resolution monochromator can be used
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background correction
two line continuum Smith-Hieftje (self reversal)
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Zeeman background correction
moderate field (10kGauss) transitions split to satellite and main absorption of atoms only occurs when polarization is parallel to magnetic field
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Questions about AAS Question: why is monochromator after the flame?
Question: What about flame light that is at the same wavelength as is being measured?
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AAS summary Advantages of AAS: very sensitive (ppb detection limits)
useful for a wide range of metals relatively inexpensive (~$30,000) When is AAS the preferred technique? Low concentration of metal ions in aqueous solution If you are interested in only a few metals (6) If sample volume is very small (<1 mL), electrothermal atomic absorption is best Disadvantages of AAS: limited dynamic range (need to know conc you are looking for) Subject to numerous types of intereference (flame and furnace)
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basic properties quantification of nearly 70 elements
ppb - weight percent microliter or microgram (furnace) milliliter (flame) biomedical, environmental, steel and metal, pharmacy, food, pollution and industrial monitoring solid liquid or gas minimal sample prep sample prep 0sec to 24hrs, measurement (seconds (flame) minutes (furnace)) no chemical info (only elemental composition) destructive more appropriate for few elements at a time (not easily applied to multielement problems) accuracy (homogeneous solution 5-10 x detn limit (accuracy ~1%) (direct solids accuracy ~5-10%) linear dynamic range usually 2 orders of magnitude (sometimes 3)
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AAS costs simple no bkgd corr ($10k) full package ($100k)
lamps (single element($150-$400) multielement($300-$400)) last ~200hrs of continuous emission gases typically run $120/year graphite tubes ($20-$50/ea) last ~200 firings heavily used system may cost $1-$2000/year for operations full service contract typically will run $6000/yr
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