|August 1, 2000; pp. 543 A-546 A|
|Copyright 2000 American Chemical Society|
Fully automated and easier-to-use systems designed for increased productivity continue to emerge.
When axial inductively coupled plasma atomic emission spectrometry (ICP-AES) hit the market in the early 1990s, some manufacturers of graphite furnace atomic absorption spectrometry (GFAAS) systems feared it was time to start looking for a new job. But despite increased pressure from ICP and other competing techniques, GFAAS continues to hold a place in the elemental analysis market.
Graphite furnace sales took a big hit about eight years ago, recalls David Pfeil of TJA Solutions. This was due to the declining environmental testing market and the introduction of axial ICP-AES, which was touted as being sensitive enough to detect low levels of elements traditionally analyzed by GFAAS, such as lead, thallium, arsenic, and selenium. ICP can do all 23 metals targeted by EPAs Contract Laboratory Program, including the four traditionally done by graphite furnace, faster than four graphite furnaces can do four elements, says Pfeil. For routine environmental testing labs, ICP-AES became an attractive alternative to GFAAS. From 1993 to 1997, AA sales in North America dropped significantly, says Bob Clifford of Shimadzu. ICP prices dropped, and in response, AA prices dropped. Today, a low-end ICP-AES system costs about $50,000, which overlaps with the upper end of the GFAAS range ($35,00060,000).
The AA market began to rebound when analysts realized that the increase in sensitivity gained by axial ICP came at the cost of increased interferences, says Glen Carnrick of PerkinElmer Instruments. Graphite furnace sales have actually started to pick up again. They havent come back to what they were, but they now remain quite steady, he says. As for competition with ICPMS, there will be pressure if the manufacturer can figure out how to make an ICPMS that performs well for about $90,000, Carnrick adds. But for now, ICPMS still remains in a class of its own, with conventional quadrupole systems starting at about $150,000 (Anal. Chem. 1999, 71, 811 A815 A).
In contrast to flame AAS, which has had little improvement in detection limits and performance over the past 1015 years, GFAAS continues to improve even to this day, albeit slower now that it is a mature market, says Carnrick. To find out just what improvements have been made recently, Analytical Chemistry surveyed several GFAAS manufacturers. Although not comprehensive, a summary of selected commercially available GFAAS systems in North America is given in Table 1. The GFAAS market in Asia and Europe encompasses manufacturers not included in this review.
But the same issues that apply to ICP-AES (Anal. Chem. 1998, 70, 211 A215 A) with regard to CTDs, also apply to GFAAS. Photomultiplier tubes (PMTs) are generally more sensitive and linear than CTDs, and not all manufacturers are convinced that the speed, flexibility, and multiplex advantage of solid-state detectors are worth the compromise.
GFAAS typically involves a minimum of four stagesdrying (to remove water), pyrolysis (to remove matrix interferents), atomization (to vaporize the metal analyte), and cleaning (to remove leftover residue). Traditionally, a simple mirror assembly is used to look inside the graphite furnace tube during the various stages to aid in method development. Some manufacturers now offer GFAAS systems equipped with a CCD camera, which continuously records images of the events taking place inside the tube.
We show a live picture of what is going on inside the furnace at all times, says Sally Dowling of GBC Scientific. The real benefit is that you can watch how the sample dries and how the gases evolve during pyrolysis, says TJA Solutions Pfeil. If the sample gets too hot and boils, it will splatter and end up outside the cuvette, resulting in a loss of signal, he says. The CCD images provide a way to confirm that all of the sample stayed in the tube.
The depth of the sample probe is also critical in GFAAS, particularly when using an autosampler, says Pfeil. If the probe isnt all the way at the bottom of the tube, a drop can hang on the tip, he says. With electronic sample viewing, you can look into the furnace tube and see exactly where the needle is with respect to the graphite tube. You can see how it is depositing your sample and whether the droplet is even. When the needle comes out, you can tell whether the droplet stuck to the needle or whether it stayed where you want it in the furnace, adds Dowling.
Because GFAAS is a mature technique, there havent been major technological advances in the past five years. Most improvements have centered around making GFAAS systems easier and faster to use. Features such as automated flame-to-furnace switching, self-aligning graphite furnace tubes, computer-coded source lamps (automatic wavelength and slit selection), automatic sample dilution, and automatic standard preparation are now available. Today, nearly every aspect of GFAAS has been touched by automation.
One of the big markets for graph ite furnace in the past 10 years has been blood lead analysis, says Carnrick. It is not uncommon for a state laboratory to have 610 graphite furnace systems dedicated to blood lead analysis, he says. Blood lead is a major problem. It is still one of the most important environmental health problems we have to deal with. Many states have mandatory laws for screening children for lead exposure, says Patrick Parsons of the New York State Department of Healths Lead Poisoning Laboratory. In contrast to EPAs approved standard methods for environmental laboratories, the National Committee for Clinical Laboratory Standards (NCCLS) has its own set of recommended methods for clinical laboratories. According to Parsons, who chairs the lead subcommittee for NCCLS, the GFAAS method for blood lead is so well established and validated that a consensus method has been proposed by NCCLS. To have a consensus method, the major GFAAS manufacturers had to agree on it, which is quite an accomplishment, he says. An alternative method proposed by the subcommittee for lead analysis is anodic stripping voltammetry, although future revisions could include ICPMS and newly emerging portable methods for blood lead. Graphite furnace AA spectrometry is currently attractive because of its reasonable cost and because it can be automated, adds Parsons.