

Flame Atomic Absorption Spectrometer
火焰原子吸收光谱仪
- SKU ATS-0001
- Atomic Spectroscopy
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 safety compliance (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Wavelength range | 185–900 nm |
|---|---|
| Optical system | Czerny-Turner monochromator |
| Flame types | air-acetylene, N2O-acetylene |
| Detection limit | 0.001–0.1 mg/L typical |
| Lamp turret | 4 to 8 hollow-cathode lamps |
| Background correction | deuterium or Zeeman |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <730> Plasma Spectrochemistry, USP <233> Elemental Impurities — Procedures, ICH Q3D Elemental Impurities
What is the Flame Atomic Absorption Spectrometer?
A flame atomic absorption spectrometer atomizes samples in an acetylene flame and measures atomic absorption. It is the routine, robust choice for a few elements at milligram per litre levels in water, soil, metals and beverages.
What is the Flame Atomic Absorption Spectrometer?
A flame atomic absorption spectrometer atomizes samples in an acetylene flame and measures atomic absorption. It is the routine, robust choice for a few elements at milligram per litre levels in water, soil, metals and beverages.
Overview
This instrument aspirates a liquid sample into a nebulizer and mixes it with fuel and oxidant gases in a burner head. The flame atomizes the analyte, and a hollow-cathode lamp specific to the element emits a narrow line that passes through the flame to a monochromator and detector. Absorption follows the Beer-Lambert law and is proportional to concentration after calibration. Deuterium or Zeeman background correction compensates for smoke and scattering, and a burner rotation or flow spoiler extends the linear range for concentrated samples. Common configurations include single or multi-element lamp turrets, flame emission mode for alkali metals, and autosamplers. Air-acetylene reaches about 2300 degrees Celsius for most elements, while nitrous oxide-acetylene is used for refractory elements such as aluminum, titanium and vanadium.
How does it work?
In atomic spectroscopy a sample is converted into free atoms in a flame, graphite furnace, plasma or hydride generation cell. The atoms absorb or emit light at wavelengths characteristic of each element. Atomic absorption passes a hollow-cathode lamp emission line through the atom cloud and measures the decrease in intensity according to the Beer-Lambert law. Atomic emission excites atoms in a plasma or flame and measures the light they emit as they relax. Atomic fluorescence excites atoms with a source and measures emitted light at a right angle, giving high sensitivity for hydride-forming elements. Inductively coupled plasma sources reach 6000 to 10000 K, atomizing and ionizing most elements; the resulting ions can be counted by mass spectrometry for very low detection limits. Calibration uses series of standards, internal standards, and background and matrix correction.
What are the key features?
- Air-acetylene and nitrous oxide-acetylene flame options
- Hollow-cathode lamp turret for several elements
- Deuterium or Zeeman background correction
- Automatic gas control and safety interlocks
- Optional autosampler for routine sequences
- Flame emission mode for alkali and alkaline earth metals
What are the technical specifications?
A typical flame atomic absorption spectrometer configuration offers wavelength range of 185–900 nm, optical system of Czerny-Turner monochromator, flame types of air-acetylene, N2O-acetylene, detection limit of 0.001–0.1 mg/L typical, lamp turret of 4 to 8 hollow-cathode lamps and background correction of deuterium or Zeeman. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Flame Atomic Absorption Spectrometer is used in trace metals in drinking water and wastewater, soil and plant nutrient analysis, metal alloy composition checks and beverage and food mineral content. Across the wider Atomic Spectroscopy class, laboratories also deploy it for elemental impurity testing of pharmaceutical materials, trace metals in drinking water, wastewater and soil and food safety and nutritional element analysis.
Which standards and certifications apply?
Relevant standards and methods include USP <730> Plasma Spectrochemistry, USP <233> Elemental Impurities — Procedures, ICH Q3D Elemental Impurities, ISO 11885 Water quality — ICP-OES determination of elements, ISO 17294-2 Water quality — ICP-MS determination of elements, US EPA Method 200.7, US EPA Method 200.8, ISO/IEC 17025 and IEC 61010-1. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 safety compliance; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Atomic spectroscopy installations need gas supplies, extraction and, for plasma systems, argon of high purity and substantial electrical power. Acetylene and nitrous oxide require proper regulators, flashback arrestors and ventilation. Sample preparation by acid digestion is a major source of error and contamination, so ultrapure acids and clean vessels are essential. Hollow-cathode lamps have limited life and may need warm-up and alignment. Background correction, internal standards and matrix matching control interferences from easily ionized elements, molecular species and viscosity. Verify performance daily with calibration standards and check stability with a continuing calibration verification. Maintain service records and monitor lamp, torch and graphite tube usage.
How do I select the right Flame Atomic Absorption Spectrometer?
Select a flame AAS when the target list is short, concentrations are in the milligram per litre range and low operating cost and simplicity matter. Specify the elements, expected concentration ranges, matrix and gases available. Confirm the burner configuration suits your matrix, since high dissolved solids can clog nebulizers, and that safety interlocks meet local gas regulations.
How does it compare with other Atomic Spectroscopy variants?
Choose the atomic technique by element, concentration and matrix. Flame atomic absorption is simple, robust and suited to milligram per litre levels in routine water, soil and metal samples. Graphite furnace atomic absorption reaches microgram per litre and below for a limited number of elements with small sample volumes. Inductively coupled plasma optical emission handles multi-element analysis at microgram per litre to percent levels with wide linear range. Inductively coupled plasma mass spectrometry reaches nanogram per litre and below for most elements and can measure isotopes. Atomic fluorescence is efficient for mercury, arsenic, selenium and antimony after hydride generation. Microwave plasma emission is an alternative to flame for some elements using nitrogen instead of acetylene. Confirm required detection limits, sample throughput, number of elements and available gases before selecting.
Full specifications
| Wavelength range | 185–900 nm |
|---|---|
| Optical system | Czerny-Turner monochromator |
| Flame types | air-acetylene, N2O-acetylene |
| Detection limit | 0.001–0.1 mg/L typical |
| Lamp turret | 4 to 8 hollow-cathode lamps |
| Background correction | deuterium or Zeeman |
| Nebulizer | high-efficiency metal or inert |
| Sample uptake rate | 4–6 mL/min |
| Gas control | automatic with interlocks |
| Interface | USB / RS-232 |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Trace metals in drinking water and wastewater
- Soil and plant nutrient analysis
- Metal alloy composition checks
- Beverage and food mineral content
Key features
- Air-acetylene and nitrous oxide-acetylene flame options
- Hollow-cathode lamp turret for several elements
- Deuterium or Zeeman background correction
- Automatic gas control and safety interlocks
- Optional autosampler for routine sequences
- Flame emission mode for alkali and alkaline earth metals
Frequently asked questions about Flame Atomic Absorption Spectrometer
Flame AAS works well for copper, zinc, iron, manganese, lead, cadmium, calcium, magnesium, sodium and potassium at milligram per litre levels. Refractory elements such as aluminum, titanium and vanadium need the hotter nitrous oxide-acetylene flame. Elements that form stable gaseous hydrides are often better measured by other techniques.
Rotating the burner head shortens the path length through the flame, reducing absorbance so that concentrated samples remain within the linear range. This extends the working range without dilution, saving time and reducing contamination risk. The angle must be reproduced exactly because absorbance depends on path length.
Drift usually comes from burner and nebulizer deposits, changing gas flows, lamp aging and room temperature shifts. Regular cleaning of the burner and nebulizer, warm-up of lamps, checks of gas pressure and calibration verification during runs control it. A drift check and recalibration trigger should be defined in the method.
Choose flame AAS for a few elements at milligram per litre levels with simple, low-cost operation. Choose graphite furnace AAS for microgram per litre trace levels with small samples. Choose ICP-OES for simultaneous multi-element work from microgram per litre to percent. Choose ICP-MS when the lowest detection limits or isotope ratios are required, accepting higher cost and matrix sensitivity.
Atomization produces smoke, molecular species and scattering that absorb or emit light unrelated to the analyte, which biases results if uncorrected. Deuterium, Zeeman or Smith-Hieftje correction subtracts these contributions. Matrix modifiers and standard addition further reduce structured background, particularly in graphite furnace analyses of complex samples.
Most samples need digestion or extraction to release the analytes and reduce matrix effects. Acid digestion in a closed vessel or microwave system is common, followed by dilution to a suitable acid concentration. Clean vessels, ultrapure reagents and method blanks control contamination. Solid samples measured by graphite furnace may need only suspension or slurry preparation in some methods.
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