Name: aas sample prep and calibration
Uploaded: 2024-12-05T18:32:15.000Z
Duration: 1 min 21 s
Channel: JoVE

Dans les mesures d’absorption atomique, les échantillons solides sont dissous dans un solvant approprié pour former une solution claire avant l’atomisation.
Les échantillons insolubles sont digérés avec des acides minéraux chauds, soit sur une plaque chauffante, soit par chauffage par micro-ondes.
D’autres méthodes pour obtenir des solutions claires comprennent l’oxydation de l’échantillon avec des réactifs liquides, sa combustion dans des récipients fermés ou sa fusion avec des réactifs à haute température.
L’utilisation de solvants organiques de faible poids moléculaire améliore l’efficacité du nébuliseur et les niveaux d’absorbance, tandis que l’extraction de solutions aqueuses en solvants non miscibles à l’eau réduit les interférences matricielles.
Des courbes d’étalonnage utilisant plusieurs solutions étalons mettant en tableau la concentration de l’analyte sont nécessaires pour déterminer la relation linéaire absorbance-concentration dans cette plage de concentration.
La méthode d’addition d’étalons, qui consiste à ajouter une portion d’échantillon à une solution étalon, est utilisée pour identifier et réduire au minimum les interférences de la matrice.
Les limites de détection typiques de l’AAS varient en fonction de la technique d’atomisation : entre 1 et 20 ng/mL pour l’atomisation à la flamme, et allant de 2 à 10 pg/mL pour l’atomisation électrothermique.

spectroscopie d'absorption atomique: laboratoire

Atomic Absorption Spectroscopy: Lab

Pour les mesures AAS, les échantillons doivent être introduits sous forme de solutions claires, ce qui nécessite souvent un traitement préliminaire approfondi pour dissoudre des matériaux tels que les sols, les tissus animaux et les minéraux. Les méthodes courantes de préparation des échantillons comprennent le traitement avec des acides minéraux chauds, la calcination humide, la combustion dans des récipients fermés, la calcination à haute température ou la fusion avec des réactifs.

Les solutions contenant des solvants organiques, tels que les alcools, les esters ou les cétones de faible masse moléculaire, améliorent les absorbances en augmentant l'efficacité du nébuliseur et en favorisant l'évaporation rapide du solvant. L'utilisation de solvants non miscibles comme la méthylisobutylcétone peut extraire les chélates d'ions métalliques, améliorant ainsi la sensibilité et réduisant les interférences des composants de la matrice.

L'étalonnage est crucial dans l'AAS, car les courbes d'absorption en fonction de la concentration sont souvent non linéaires. Des courbes d'étalonnage périodiques et l'utilisation de solutions étalons encadrant la concentration de l'analyte sont nécessaires pour une analyse précise. La méthode d'ajout d'étalon est couramment utilisée pour compenser les interférences chimiques et spectrales causées par la matrice de l'échantillon.

Il est important de noter que les limites de détection dans l'AAS varient en fonction de la technique d'atomisation. L'atomisation par flamme a des limites de détection allant de 1 à 20 ng/mL, tandis que l'atomisation électrothermique a des limites de détection comprises entre 0,002 et 0,01 ng/mL. L'analyse d'absorption atomique par flamme a généralement une erreur relative de quelques pour cent, qui peut être réduite avec des précautions spéciales. Les erreurs dans l'atomisation électrothermique sont généralement 5 à 10 fois plus élevées que celles de l'atomisation par flamme.

Spectroscopie d'absorption atomique: laboratoire

Pour les mesures AAS, les échantillons doivent être introduits sous forme de solutions claires, nécessitant souvent un traitement préliminaire important pour dissoudre des matériaux tels que les sols, ...

Education

Enseignement

JoVE Core

Analytical Chemistry

Chimie analytique

Unit 1

Unité 1

Atomic Spectroscopy

Spectroscopie atomique

KEY TERMS AND CONCEPTS

TERMES ET CONCEPTS CLÉS

aas sample prep and calibration

Atomic absorption spectroscopy (AAS) depends on careful sample preparation and calibration. Samples must be turned into clear solutions before measurement. That often means extra treatment to dissolve materials such as soils, animal tissues, and minerals.

Common sample prep methods include hot mineral acids, wet ashing, combustion in closed containers, high-temperature ashing, and fusion with reagents. These steps help make the sample suitable for AAS analysis. Solutions that contain organic solvents, such as low-molecular-mass alcohols, esters, or ketones, can also increase absorbance. They do this by improving nebulizer efficiency and helping the solvent evaporate faster.

Immiscible solvents like methyl isobutyl ketone can be used to extract chelates of metallic ions. A chelate is a complex that helps separate the metal from other material in the sample. This can improve sensitivity and reduce interference from matrix components, which are the other substances present in the sample.

Calibration is especially important in AAS because absorbance does not always change linearly with concentration. For accurate results, scientists use periodic calibration curves and standard solutions that bracket the analyte concentration. The standard-addition method is also common. It helps correct for chemical and spectral interferences caused by the sample matrix.

Detection limits in AAS depend on the atomization technique. Flame atomization has detection limits of about 1 to 20 ng/mL. Electrothermal atomization is more sensitive, with detection limits around 0.002 to 0.01 ng/mL. Flame atomic absorption analysis usually has a relative error of a few percent. With special precautions, this can be reduced. Errors in electrothermal atomization are usually 5 to 10 times higher than in flame atomization.

AAS Sample Prep and Calibration

atomic spectroscopy: absorption, emission, and fluorescence

atomic-spectroscopy-absorption-emission-and-fluorescence

Element Analysis with Atomic Light Spectra

Atomic spectroscopy is used to identify and measure elements by their light signals. It supports both qualitative analysis, which tells what is present, and quantitative analysis, which tells how much is present. The optical methods in this group are atomic absorption spectroscopy, atomic emission spectroscopy, and atomic fluorescence spectroscopy. These methods begin with atomization. In this step, a solid, liquid, or solution sample is changed into gas-phase atoms and ions. Once the sample...

atomic spectroscopy: effects of temperature

atomic-spectroscopy-effects-of-temperature

How Heat Changes Atomic Spectra

Heat changes atomic spectra by affecting atomization, excitation, ionization, and line shape. In atomic spectroscopy, atomization means converting a sample into gas-phase atoms and ions. The flame temperature needed for this step changes how efficiently the method works and shifts the balance between excited and ground-state atoms. At thermal equilibrium, the relative numbers of excited and ground-state atoms can be estimated with the Maxwell-Boltzmann distribution. A small temperature rise...

atomic absorption spectroscopy: overview

Atomic Absorption Spectroscopy for Trace Metals

Atomic absorption spectroscopy (AAS) measures trace metals by tracking how atoms absorb electromagnetic radiation (EMR). The absorbed light makes atoms move to a higher-energy orbit. In AAS, the key step is atomization, which converts the sample into gas-phase atoms. A flame or a furnace is typically used for this step. Inside the flame, some atoms become thermally excited. Most stay in the ground state, which is the lowest-energy state. These ground-state gas-phase atoms absorb EMR only when...

atomic absorption spectroscopy: instrumentation

atomic-absorption-spectroscopy-instrumentation

Atomic Absorption Spectroscopy: Key Parts

Atomic absorption spectrophotometry uses a set of key parts to measure light absorbed by atoms. The main components are a radiation source, an atomizer, a monochromator, and a detector. Each part has a specific job in the instrument. The radiation source is usually a hollow-cathode lamp, or HCL, or an electrodeless-discharge lamp, or EDL. Both produce a narrow emission line at the needed wavelength. Some instruments instead use continuum sources with high-resolution monochromators to narrow...

atomic absorption spectroscopy: radiation and light sources

atomic-absorption-spectroscopy-radiation-and-light-sources

Choosing Light Sources for AAS Measurements

Atomic absorption spectroscopy (AAS) uses a light source that emits a very narrow range of wavelengths. This is needed because the source must match the absorption behavior of the analyte atom. The choice of source also depends on giving a precise, intense emission at the right wavelength for accurate detection. Two common line sources in AAS are hollow-cathode lamps (HCLs) and electrodeless-discharge lamps (EDLs). These lamps are selected based on the element being analyzed and the level of...

atomic absorption spectroscopy: atomization methods

atomic-absorption-spectroscopy-atomization-methods

Atomic Absorption Spectroscopy: Sample Atomization

Atomic absorption spectroscopy uses sample atomization to turn a liquid specimen into free atoms for analysis. The two main approaches are flame atomization and electrothermal atomization. Both methods prepare the sample so its atoms can be measured by the instrument. Flame atomization uses a nebulizer and spray chamber to mix the sample with a fuel-oxidant mixture. This creates a fine aerosol mist that enters the burner. The fuel and oxidant are usually close to a stoichiometric ratio, but a...

atomic absorption spectroscopy: interference

atomic-absorption-spectroscopy-interference

Correcting Errors in Atomic Absorption Spectroscopy

Atomic absorption spectroscopy interference can create systematic error by making the analytical signal or the background look stronger or weaker than it should be. In atomic absorption measurements, these errors are usually grouped as spectral interference, chemical interference, and physical interference. Spectral interference happens when signals from other elements or molecules overlap with the analyte signal, the substance being measured. This overlap can falsely raise or hide the analyte...

atomic absorption spectroscopy: lab

Atomic absorption spectroscopy (AAS) depends on careful sample preparation and calibration. Samples must be turned into clear solutions before measurement. That often means extra treatment to dissolve materials such as soils, animal tissues, and minerals. Common sample prep methods include hot mineral acids, wet ashing, combustion in closed containers, high-temperature ashing, and fusion with reagents. These steps help make the sample suitable for AAS analysis. Solutions that contain organic...

atomic emission spectroscopy: overview

Atomic Emission Spectroscopy for Element Analysis

Atomic emission spectroscopy is used to identify the elements in a sample by measuring the light they emit. Atoms are first excited to higher energy levels by thermal energy from hot sources such as plasma, arcs, or sparks. When they fall back to lower energy levels, they give off light at specific wavelengths. Each element produces its own set of lines, so the emission spectrum can show both what is present and how much is there. AES instruments are similar to atomic absorption spectrometers,...

atomic emission spectroscopy: instrumentation

atomic-emission-spectroscopy-instrumentation

AES Sample Handling and Detection

Atomic emission spectrometry (AES) uses sample handling, atomization, and detection parts to measure emitted light from atoms and ions. The sample must first be changed into a gas-phase form so it can produce a measurable signal. AES uses two main atomizer types. Continuous atomizers, such as flames and plasmas, feed the sample in a steady stream. Discrete atomizers add one sample at a time with syringes or autosamplers. The electrothermal atomizer is the most common discrete type. Many...

atomic emission spectroscopy: interference

atomic-emission-spectroscopy-interference

Reducing Interference in AES Signals

Atomic emission spectroscopy (AES) can produce interfering signals when atoms and molecules in a flame or plasma emit overlapping light. High-temperature atomizers excite many species at once, including oxides, hydroxides, and flame combustion products. These extra emissions can make the analyte signal harder to read. Spectral interference happens when emission lines or bands overlap. One way to reduce it is to improve instrument resolution. Another is to choose a different emission line for...

inductively coupled plasma atomic emission spectroscopy: principle

inductively-coupled-plasma-atomic-emission-spectroscopy-principle

ICP-AES Torch and Sample Analysis

Inductively coupled plasma atomic emission spectroscopy uses a plasma torch to analyze elements in a sample. This method is also called inductively coupled plasma optical emission spectroscopy, or ICP-OES. It is widely used because the plasma creates a strong environment for elemental analysis. The ICP source, or torch, contains three concentric quartz tubes. Argon gas flows through the tubes. A spark from a Tesla coil starts the ionization of argon and creates a high-temperature plasma. The...

inductively coupled plasma atomic emission spectroscopy: instrumentation

inductively-coupled-plasma-atomic-emission-spectroscopy

ICP-AES Instrument Types and Detection

Inductively coupled plasma atomic emission spectroscopy, or ICP-AES, uses an inductively coupled plasma to detect and analyze elements in a sample. The method measures the light given off by atoms, which helps identify and compare different elements. It is a common approach in atomic emission spectroscopy. ICP-AES instruments are built in three main forms: sequential, simultaneous multichannel, and Fourier transform instruments. Fourier transform designs are less commonly used, but they are...

atomic emission spectroscopy: lab

Plasma Sources in Atomic Emission Spectroscopy

Atomic emission spectroscopy uses plasma sources to identify elements by their light. The method creates abundant spectra with characteristic emission lines. Inductively coupled plasma, or ICP, is especially useful because it gives strong quantitative data. It works well under stable conditions, with low noise, low background, and few interferences. Newer air-operated microwave sources are also being studied. These sources may be more cost-effective than conventional ICP systems. Atomic...

atomic fluorescence spectroscopy

Measuring Elements by Atomic Fluorescence

Atomic fluorescence spectroscopy measures elements by detecting the light atoms give off after they are excited by electromagnetic radiation. The atoms are first placed in a flame, furnace, or plasma. They absorb energy, become excited, and then release that energy as they return to their original state. The emitted light is called fluorescence. The fluorescence is observed at a right angle to the incoming beam. This setup helps separate the emitted light from the light used to excite the...

flame photometry: overview

Flame Emission Spectrometry Basics

Flame emission spectrometry uses a flame to excite elements in a sample so their light can be measured. It is also called flame photometry. The method can be used for both qualitative and quantitative analysis of elements. The idea became established in the early 1860s when Kirchhoff and Bunsen showed that specific elements give off characteristic radiation in a flame. The first instrument for this purpose measured sodium in plant ash with a Bunsen flame. A major problem was how to add the...

flame photometry: lab

Flame Photometry and Metal Detection

Flame photometry is a method for detecting metals by measuring the light they emit in a flame. A solution such as potassium chloride is aspirated into the flame. The solvent evaporates first. The remaining salt becomes dehydrated and then dissociates into free gaseous atoms in the ground state. Some of these atoms absorb energy from the flame and move to an excited state. When they return to the ground state, they emit photons at characteristic wavelengths. These emissions are very narrow...

key terms and concepts

Learn how AAS samples are prepared, why calibration curves matter, and how flame and electrothermal atomization affect detection limits and error.

AAS Sample Prep and Calibration | JoVE K12

analytical chemistry

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AAS Sample Prep and Calibration

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