

Transverse-Heated Graphite Furnace Atomic Absorption Spectrometer
横向加热石墨炉原子吸收光谱仪
- SKU GFA-0001
- Graphite Furnace AAS
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- 21 CFR Part 11 software compliance (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Atomizer | transverse-heated graphite tube |
|---|---|
| Maximum temperature | 3000 °C |
| Heating rate | up to 2000 °C/s |
| Platform | L'vov platform standard |
| Detection limit | 0.01–1 µg/L typical |
| Background correction | Zeeman effect |
By Lab Manufacturers China Technical TeamLast reviewed Standards: Ph. Eur. 2.2.22 Atomic absorption spectrometry, USP <852> Atomic Absorption Spectroscopy, US EPA Method 7010 Graphite furnace atomic absorption spectrophotometry
What is the Transverse-Heated Graphite Furnace Atomic Absorption Spectrometer?
A transverse-heated graphite furnace AAS applies current across the whole tube length for a more uniform temperature. It is chosen when peak reproducibility and freedom from condensation and memory interferences matter most in trace analysis.
What is the Transverse-Heated Graphite Furnace Atomic Absorption Spectrometer?
A transverse-heated graphite furnace AAS applies current across the whole tube length for a more uniform temperature. It is chosen when peak reproducibility and freedom from condensation and memory interferences matter most in trace analysis.
Overview
In transverse heating the tube is clamped at its ends and current flows across the tube wall rather than along its length, so the entire tube reaches a nearly uniform temperature. This reduces the cool ends that cause analyte condensation and memory effects in end-heated designs, giving better peak shape and reproducibility, especially for refractory and carbide-forming elements. The design also allows a platform to be used effectively because the platform and tube reach similar temperatures, which delays atomization until the gas phase is uniform and reduces interference. Temperature control is fast and precise, and tubes tolerate high atomization temperatures. Because the tube geometry is more complex, tubes and the power supply may cost more. The platform is standard equipment, and Zeeman correction is typically integrated for difficult matrices.
How does it work?
A measured aliquot of sample, typically 5 to 50 microlitres, is deposited into a graphite tube through a dosing hole. The tube is heated in programmed stages: drying to evaporate solvent, pyrolysis to remove organic and inorganic matrix, atomization at high temperature to create a transient cloud of free atoms, and cleaning to remove residue. A hollow-cathode lamp emits the element resonance line through the tube, and the detector records a transient absorbance peak whose area is proportional to the analyte mass. Because atomization is efficient and atoms remain in the optical path longer than in a flame, detection limits are far lower, often in the nanogram per litre range for cadmium and lead. Strong background correction by Zeeman effect or deuterium lamp is essential, and matrix modifiers stabilize analytes during pyrolysis. Tubes and platforms are consumables, and temperature programs are optimized for each matrix.
What are the key features?
- Current applied transversely across the tube wall
- Uniform tube temperature and improved peak shape
- L'vov platform as standard for stabilized atomization
- Reduced condensation and memory effects
- Fast, precise temperature control to 3000 °C
- Integrated Zeeman background correction
What are the technical specifications?
A typical transverse-heated graphite furnace atomic absorption spectrometer configuration offers atomizer of transverse-heated graphite tube, maximum temperature of 3000 °C, heating rate of up to 2000 °C/s, platform of L'vov platform standard, detection limit of 0.01–1 µg/L typical and background correction of Zeeman effect. 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 Transverse-Heated Graphite Furnace Atomic Absorption Spectrometer is used in ultratrace metals in complex water matrices, refractory and carbide-forming elements, pharmaceutical elemental impurities and clinical trace element measurement. Across the wider Graphite Furnace AAS class, laboratories also deploy it for trace metals in drinking water and wastewater, lead and cadmium in food, blood and urine and elemental impurities in pharmaceutical materials.
Which standards and certifications apply?
Relevant standards and methods include Ph. Eur. 2.2.22 Atomic absorption spectrometry, USP <852> Atomic Absorption Spectroscopy, US EPA Method 7010 Graphite furnace atomic absorption spectrophotometry, ISO 15586 Water quality — Determination of trace elements by graphite furnace AAS, ICH Q2(R2) Validation of analytical procedures and IEC 61010-1. Certification candidates for this model are CE, ISO 9001 manufacturing and 21 CFR Part 11 software compliance; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Graphite furnace systems need argon of high purity, a stable power supply, temperature-controlled cooling and adequate exhaust for pyrolysis vapors. Acid digestion or dilution precedes most measurements, and ultrapure reagents and clean vessels are essential because contamination is visible at nanogram per litre levels. Matrix modifiers must be prepared accurately and dosed reproducibly. Operating cost is dominated by graphite tubes, platforms and lamps, so tracking firings and sensitivity helps schedule replacement. Daily checks include autosampler alignment, blank levels and calibration verification. Because each matrix behaves differently, temperature programs require development and should be fixed in the method with defined acceptance criteria.
How do I select the right Transverse-Heated Graphite Furnace Atomic Absorption Spectrometer?
Select a transverse-heated furnace when reproducibility, freedom from memory effects and accurate analysis of refractory elements are priorities, especially in difficult matrices. Specify the elements, required detection limits, matrices and modifiers. The higher tube cost is justified by better platform performance and longer method robustness.
How does it compare with other Graphite Furnace AAS variants?
Choose a graphite furnace system when trace or ultratrace detection limits are required for a limited number of elements and sample volumes are small. Transverse-heated tubes give more uniform temperature and better reproducibility, while end-heated tubes are simpler and less costly. Zeeman background correction is preferred for complex matrices that produce high structured background. An autosampler with modifier dosing and automatic dilution is important for throughput and for reproducible standard addition. Simultaneous multi-element instruments reduce analysis time when several elements are required, but single-element sequential operation remains the most common and lowest-cost approach. Confirm the graphite tube type and coating suit your elements, since carbide-forming elements such as silicon and vanadium require special tubes.
Full specifications
| Atomizer | transverse-heated graphite tube |
|---|---|
| Maximum temperature | 3000 °C |
| Heating rate | up to 2000 °C/s |
| Platform | L'vov platform standard |
| Detection limit | 0.01–1 µg/L typical |
| Background correction | Zeeman effect |
| Sample volume | 5–50 µL |
| Temperature program steps | up to 20 |
| Purge gas | argon, 200–300 mL/min |
| Tube life | 500–2000 firings |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Ultratrace metals in complex water matrices
- Refractory and carbide-forming elements
- Pharmaceutical elemental impurities
- Clinical trace element measurement
Key features
- Current applied transversely across the tube wall
- Uniform tube temperature and improved peak shape
- L'vov platform as standard for stabilized atomization
- Reduced condensation and memory effects
- Fast, precise temperature control to 3000 °C
- Integrated Zeeman background correction
Frequently asked questions about Transverse-Heated Graphite Furnace Atomic Absorption Spectrometer
In end-heated tubes the center is hotter than the ends, so analyte vapor can condense at the cool ends and re-atomize later, causing broad, tailing peaks and memory effects. A transversely heated tube avoids this gradient, giving sharper peaks, better reproducibility and fewer carry-over problems between samples.
A platform is a small graphite plate inside the tube on which the sample is placed. It heats mainly by radiation from the tube wall, so atomization occurs after the tube and gas phase have stabilized at a uniform temperature. This delays atomization, reduces interference from the matrix gas and improves accuracy for volatile elements.
Transverse-heated tubes can require higher current and a more capable power supply to heat the whole tube quickly and uniformly, adding cost and electrical demand. In return, temperature control is uniform and reproducible. Confirm the laboratory electrical service supports the instrument and its cooling unit.
Detection limits are commonly 0.01 to 1 microgram per litre for many elements, with cadmium and lead at the lower end using 20 microlitre injections. Larger injection volumes, preconcentration or a platform can improve limits further. Detection limits depend on matrix, tube condition, lamp and the temperature program used.
Pyrolysis leaves residual matrix that produces high, structured background and smoke during atomization. Zeeman correction measures background very close to the analyte line and handles this structured background well, whereas deuterium correction can be inadequate when background is high or rapidly changing. That is why Zeeman systems dominate difficult matrices.
Optimize drying to avoid spattering, then increase pyrolysis temperature until analyte loss begins, and set atomization as low as possible for a sharp, complete peak without tailing. Cleanout must remove residue without shortening tube life. Modifier choice, observation of peak shape and recovery from spiked samples guide each step.
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高通量自动进样石墨炉原子吸收光谱仪
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