iCE™ 3500 AAS Atomic Absorption Spectrometer
iCE™ 3500 AAS Atomic Absorption Spectrometer
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Thermo Scientific™

iCE™ 3500 AAS Atomic Absorption Spectrometer

For the best of all AA worlds, the dual Flame & Furnace iCE™ 3500 AAS from Thermo Scientific™ delivers exceptional elemental analysis.
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Catalog NumberDescription
942350023500iCE 3500 Double Beam Dual Atomiser AA Spectrometer
942350023501iCE 3500 AA Spectrometer with 100 mm Burner
Catalog number 942350023500
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Description:
iCE 3500 Double Beam Dual Atomiser AA Spectrometer

The Thermo Scientific™ iCE™ 3500 AAS provides unrivalled performance, flexibility and simplicity. The innovative dual atomizer design enables safe, software-controlled switching between flame and furnace analysis with a single mirror movement. The high precision, double beam optics, combined with an Echelle monochromator produce low detection limits and long term analytical stability. Unique Quadline deuterium background correction with guaranteed performance is provided as standard. The flame atomizer design incorporates a 50 mm titanium burner with improved solids capability to increase the efficiency and accuracy of your flame analysis.The furnace atomizer includes GFTV, a furnace vision system which improves efficiency and simplifies method development by providing a high definition, real time video of the inside of the cuvette.

Maximize Productivity

This combined Flame and Furnace AAS system, delivers a complete solution for laboratories facing challenging detection limits and needing high through-put sample capacity.
  • Software-controlled changeover from flame to furnace analysis, without an operator even in the room
  • Run unattended, automated analysis with fully configurable auto-sampler
  • SOLAAR software provides incredible support with wizards, optimization routines and automated performance controls
  • Six lamp auto-aligning carousel for maximum light throughput

Gain Cost Efficiency

Gain even greater efficiency from hardware and accessories designed for cost efficiency.
  • Innovative Extended Lifetime Cuvettes (ELC) for reduced consumable costs, can be used for thousands of firings
  • Run analysis with just micro-liters of sample to minimize consumable consumption
  • Gas flows with intelligent software controls keep gas usage to a minimum
  • GFTV real time viewing enables precise analysis, time after time

Enjoy Advanced Performance and Flexibility

All the innovation, performance and ease of use you expect from Thermo Scientific instruments come with the iCE3500 AAS.
  • The unique dual atomizer design provides a second sample compartment where the furnace can be left permanently aligned and ready for use
  • D2 background correction for flame and furnace analysis as standard
  • Zeeman background correction available for furnace work, from the optional Thermo Scientific™ GFS35Z™ furnace upgrade
  • Double beam optics with a dual monochromators consisting of an Echelle prism and a grating
Specifications
TypeAtomic Absorption Spectrometer
Background CorrectionGuaranteed Quadline Deuterium or AC Zeeman Systems
DescriptioniCE 3500 Double Beam Dual Atomiser AA Spectrometer
Flame AtomizerUniversal System (Uses 50 mm Finned Ti Burner)
Furnace Atomizer OptionGFS35 or GFS35(Z) Combined Module
Furnace Vision SystemAs Standard
Gas ManagementAutomatic Binary Control
Lamp Carousel6 Lamp-Coded, Auto-Aligning
MonochromatorEschelle Type
OpticsDouble Beam
PhotomultiplierWide Range (180 to 900 nm)
Unit SizeEach

Frequently asked questions (FAQs)

What is a segmented flow sample introduction system and how can it help me?

Segmented flow sample introduction systems are a very helpful tool to increase the productivity in your laboratory. Such devices work with a valve system that enables fast uptake of the sample to the plasma, and minimize the wash out times between different samples. Therefore, the time required for analysis can be shortened considerably. An example for such a system is the sprint valve system available on the Thermo Scientific iCAP 7600 ICP-OES (https://www.thermofisher.com/order/catalog/product/842320076121).

Can slurry nebulization be used with pharmaceutical products?

Slurry nebulization is more commonly used in environmental testing applications. In principle, slurry nebulization can be used for pharmaceutical testing and there have been studies done on this. Obviously particle size is a key factor here - the smaller the particles the better. However, it is also worth pointing out that the method preferred by USP is microwave digestion.

When analyzing elemental impurities in phramaceutical samples, how is the method detection limit calculated and how is it related to the parameter instrumental detection limit and blank equivalent concentration?

The parameters BEC, LOD, and LOQ are frequently used to describe the detection capabilities of an analytical instrument. The acronym BEC abbreviates the parameter blank equivalent concentration. This value refers to the “apparent concentration”, and is composed of the contamination level in the blank, any residual interference signal, and the instrument background (from the detection system). The parameter instrumental detection limit (IDL, often referred to as Limit of Detection, LOD) is defined as the limit of detection that can be achieved by the instrument used. This amount is typically defined as a quantity that gives a distinguishable signal in the detection system. The common definition for the IDL is based upon the standard deviation (LOD = 3.3 x standard deviation of the regression line of calibration curve) of a blank sample measured in the beginning of a calibration curve, or a minimum signal to noise ratio of 3:1. Both parameters, BEC and IDL are automatically calculated by Thermo Scientific Qtegra Intelligent Scientific Data Solution (ISDS) platform software (https://www.thermofisher.com/order/catalog/product/IQLAAEGABSFAOVMBCZ). In contrast, on the IDL, the parameter method detection limit (MDL) includes the extent of all dilution steps carried out during the sample preparation. The MDL is typically based upon a blank solution that has been prepared according to the preparation procedure that is being used to prepare all the samples. In situations where there is no sample preparation or if the preparation involves a single dilution step, MDLs might be calculated based on the standard deviation of a low level standard. MDL concentrations are always more conservative than IDL concentrations.

How does the format of my sample impact dilution when analyzing elemental impurities in pharmaceutical drug products?

If samples are in solid form, the dilution incurred will be dictated by the digestion procedure being used to prepare the sample for analysis. If samples are being analyzed in their native form or after simple dilution, there may be more flexibility in the dilution factor used during preparation. Regardless of the sample's original form, the sample matrix must contain a tolerable level of dissolved solids prior to introducing it into the instrument. If an ICP-MS is being used for analysis, the sample matrix should contain 0.2% TDS or, if no special configuration for the sample introduction system is used (e.g., utilizing AGD).

What is the best choice for an internal standard to be used with pharmaceutical samples?

Internal standards are used in many applications to correct for potential drifts in instrumental sensitivity over time or changes in the sample matrix. The selection of a suitable internal standard should include the following aspects: - The internal standard should have a first ionization potential similar to the analyte, and should have a similar mass as the analyte.
- The internal standard must not be part of the sample.
- It should not generate or be affected by spectral interferences.
- It should be at a low and uniform (preferably zero) concentration in all samples.

Although ICP-MS is a technique considered by some to be relatively robust with respect to matrix effects, in reality, matrix effects do commonly exist and the use of internal standards is standard practice. Internal standards also help account for changes in the transport efficiency of the sample through aerosol.