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7200CTS Cryogen-Free Preconcentrator

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Entech is proud to release the world’s first multi-capillary column trapping system (MCCTS) patent pending, for the precise concentration of vapor phased volatile chemicals in the range of C3 to C18 without the need for liquid nitrogen or complicated electronic cooling. With over 28 years of continued improvements and industry feedback, the 7200CTS is as established and reliable as it is new and improved. Many of the important advancements that have led to its unparalleled reproducibility, such as quantitative volumetric measurements utilizing “Accu-Sample Technology,” and digital valve isolation, are left unchanged. The core trapping system, however, has been completely reengineered, giving way to a technology that will likely replace the utilization of packed traps for most, if not all methods requiring the preconcentration of vapor phase volatile organic compounds.

Improved Performance And Dynamic Range For EPA Method TO-15 using the Entech 7200 and Agilent 7890B/5977 GCMS

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Canister sampling and analysis for measurement of volatile chemicals is finding use in a growing number of diversified applications. This has required air laboratories to accommodate an even wider dynamic range of sample concentrations, and a growing list of compounds to include those once thought to be incompatible with canister sampling techniques. New materials for the internal lining of canisters and field sampling systems, as well as laboratory analyzers optimized using 3D Computer Assisted Design software have provided the improved performance needed to meet these challenges.

A new Air Toxics TO-15 Analyzer based on the Entech 7200 Preconcentrator and Agilent 7890B/5977 GCMS system is demonstrated here which improves productivity and analytical accuracy. Every aspect of the sample preparation process has been optimized to improve linearity, recovery, sensitivity, and dynamic range. Linear calibrations that meet TO-15 criteria are now possible over a dynamic range of 100-2000 fold, reducing the number of dilutions necessary, while lowering detection limits to meet today’s State driven Low Level TO – 15 Method requirements . Improvements in recovery and linearity also reduce the downtime previously caused by systems that were only marginally meeting required method linearity criteria. The following application note will describe the new advancements in the 7200/7890B/5977 TO15 Analyzer that have resulted in a dramatic improvement over prior technology.

Strong similarities between night-time deposition velocities of carbonyl sulphide and molecular hydrogen inferred from semi-continuous atmospheric observations

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We investigated the diurnal variations of atmospheric carbonyl sulphide (COS) during 2011 at Gif-sur-Yvette, a suburban atmospheric measurement site in France. These data were collected semi-continuously in parallel with hydrogen (H2), carbon monoxide (CO) and 222Radon (222Rn) measurements. Fluxes and deposition velocities were calculated for nocturnal situations of low boundary layer height using the Radon-Tracer Method. Contrary to CO and H2, the diurnal cycles of COS are not impacted by emissions from nearby automobile traffic. In the absence of local anthropogenic combustion sources, COS and H2 mole fractions generally show similar temporal variations with night-time depletion coinciding with 222Rn accumulation during stable nocturnal conditions. Nocturnal COS deposition velocities range from 0.07 to 0.40mm s_1, with an annual mean of 0.1890.12mm s_1 (n_14). We found strong similarities between COS and H2 dry deposition velocities in terms of annual mean and ranges of variation, and data showed linear correlation between the two. This study provides new evidence of the loss of COS near the ground via non-photosynthetic processes. Although the dominant sink of atmospheric H2 is diffusion and subsequent destruction in soils, it is not all certain that COS is taken up at night solely by soils.

Laboratoire des Sciences du Climat et de l’Environnement, IPSL, CEA, CNRS, UVSQ,
CE Saclay, Baˆt 703 L’Orme des Merisiers, 91191, Gif-sur-Yvette, France

7200 Operations Manual .NET

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For Service Engineers and Distributors.
A few Tech Notes will only appear in the SEND version of the manual because they would be a one time change by an engineer, the procedure or information is advanced for most users, or to provide additional information to the service engineers.

Entech 2017 Catalog

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This is the complete Entech 2017 Catalog. You can download the PDF or use our Flipbook viewer (below) for a smoother experience. Please note that not all sampling products are included. The Entech store is the best place to find photos and descriptions of every product we carry.


Cryogenic Pre-concentration Theory

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The analysis of volatile organic compounds, at levels found in urban air, requires an initial sample pre- concentration to reach the detection limits imposed by the various methods, using GC/MS.

Enrichment of organics relative to the fixed gases found in air is accomplished by passing a known volume of air through a trap that selectively retains the organics while allowing bulk gases to pass through unimpeded. If a trap packing (i.e. glass beads) has a low affinity for the targeted analytes, a reduction in the trapping temperature is required to allow quantitative retention of the VOC’s on the trap. This increases the affinity for surfaces by decreasing vibrational and kinetic energies that would otherwise keep these compounds mobile. When a very weak sorbent is used, such as glass beads, the trapping temperature must be between -100 to -180˚C depending on the list of analytes targeted. For method TO-14, a trapping temperature of -150°C is recommended. For sorbents exhibiting a higher affinity for VOC’s, such as Tenax and activated charcoal, trapping can be accomplished near or at room temperature. The stronger the sorbent, the higher the necessary desorption temperature for recovery of the trapped organics. A minimum temperature difference between trapping and desorption of 150˚C is common although stronger sorbents such as carbon molecular sieve can require desorption temperatures in excess of 300°C after ambient temperature sample collection.

To quantify the levels of VOC’s in air, the volume of sample concentrated must be determined. More accurately, since volume is temperature and pressure dependent, the mass of sample must be determined and then referenced to a volume at STP conditions. Withdrawing a known standardized volume from a canister is complicated by the varying pressures found among different canister samples. Two techniques have been developed and used routinely to measure sample volumes. The first determines the sample mass indirectly by measuring the pressure difference in a vacuum reservoir of known volume before and after sample concentration. The reservoir is placed downstream of the trap and collects the major air components (N2, O2, Ar) that do not condense in the trap. The STP volume is calculated by the formula:

VT= (PD/14.696) x VR

Where VT is volume trapped, PD is the pressure differential in the reservoir before and after sampling, and VR is the volume of the reservoir. The proper use of this technique is the ideal means for measuring volume from a sample container. Inconsistent flow measurements due to pressure differences do not occur since start and end pressures are all that are required. Using a vacuum pressure transducer to monitor the pressure in a vacuum reservoir, the flow is adjusted using a digital valve. The second technique utilizes a mass flow controller to directly measure STP standardized volume per unit time. In practice, the flow rate is converted to a volume either by waiting a required period of time or directly by integrating the actual flow output from the mass flow controller (MFC). Integrating an MFC’s output allows sample volumes to be changed and can also readily detect trapping flow rate upsets due, for example, to excessive ice formation in the primary cryogenic trap. MFC’s also allow the flow rate to remain constant during trapping. Since an MFC is not accurate below 10% of its range, however, the vacuum reservoir is often a preferred technique because smaller volumes may be accurately introduced into the trap with functionality using 10-1000cc’s of a complex gas mixture. Mass Flow Controllers are typically factory calibrated using pure nitrogen gas. It is, therefore, a good practice to dilute standards in zero air so that the “air” samples can be normalized against the standards.


Water also has to be managed when concentrating large volumes. Roughly 18 microliters (ul) of water are recovered from every liter of sample concentrated that was initially at 70 % relative humidity (RH) at 25 °C. Since typical sample sizes can be 500 cc, that would result in about 9 ul of water that could eventually end up on the analytical column and in the detector. That much water can foul up chromatographic resolution, reduce column life and degrade the performance of detectors. In particular, injections of over 1 ul of water into a typical bench top mass spectrometer will cause attenuation of analytes that co-elute with the water peak. The amount of sample at 70 % relative humidity that can be concentrated without water management/removal then is roughly 50–70 cc. That is not enough sample to monitor VOC’s at the sub parts per billion levels using an ordinary GC/MS. To eliminate water and improve chromatographic resolution, a second concentration stage is implemented which further reduces the sample volume.

VOC’s in ambient air exist at levels that are at least three to four orders of magnitude below their saturation point. Therefore, assuming there are no absorptive surfaces, VOC’s from a 1000cc sample volume should volatilize into a 1 cc volume at room temperature after concentration if allowed to come to equilibrium. If this volume is actually flushed slowly with 40 to 50cc of inert gas at room temperature, the VOC’s could be quantitatively transferred to the gas phase. This is similar to the principle behind purge and trap analysis of water samples. In the case of air, however, initial trapping of 1000 cc would only yield 15 to 20 microliters of water rather than the 5000 ul’s used in water analysis. The distribution of the condensed water on the glass beads in the trap should further facilitate the transfer of all organic compounds to the gas phase (the rate at which equilibrium is achieved).

A second three stage concentration technique called microscale purge and trap is analogous to the purge and trap used in water analysis, only on a much smaller scale. The air sample is first concentrated to about a 0.5 cc volume in a first stage cryogenic trap. The trap is then heated to roughly room temperature and held there while slowly passing helium or nitrogen through it to transfer these compounds to the secondary trap. The second trap is usually Tenax at about – 10°C. Sweeping the VOC’s from the first to the second trap with only 45 cc of helium results in a transfer of less than 1 ul of water (45 cc at 100 percent relative humidity) which can be handled quite readily by bench top mass spectrometers. After transferring the VOC’s to the second trap, they can be back flushed off while heating to be further focused on an open tubular focusing trap for rapid injection into the analytical column.

Ambient level concentrations are typically quantified in the range of 1-100 parts per billion by volume (ppbv), although blank certification is required down to 0.2 ppbv. Based on a maximum carryover of 0.1% in a well-designed system, one could expect to analyze a sample 1000 times higher than the 0.2 ppbv allowable by the ambient air method blank level and still obtain a clean blank on the subsequent run. This would easily cover the expected ambient concentrations of voc’s. However, source levels can be thousands of times still higher than this. Under such conditions, system contamination is imminent.

One or more of the following can cause carryover in a concentration system;

ad-sorption, ab-sorption, insufficient flushing between runs, and unswept zones (dead volume). Adsorption occurs if there is any affinity of the VOC’s for the surfaces to which they are exposed. This can be reduced by heating exposed surfaces as well as by utilizing inert materials.  Absorption can occur when VOC’s are exposed to polymeric materials such as Teflon and Nafion, which absorb and off gas quite readily. Carryover due to insufficient flushing can be eliminated by making sure the flushing of lines occurs all the way up to the next canister to be analyzed before concentrating a sample from it. A thin film of fused silica should line sample flow paths entirely as exposed metal oxides should not come into contact with polar compounds. Tubing with a fused silica lining does not need water to passivate the surface, so extractions in completely dry conditions will provide the same recoveries as extractions in humid conditions using a surface coated with an inert polymer. Fused silica coatings are also capable of recovering higher molecular weight compounds, as these compounds can be released by mild heating.

Worthy of more discussion is the concept of un-swept volumes within a flow system. These are volumes that are not rapidly flushed during cleanup operations because of the lack of a clear exit flow path. The most commonly found un-swept zones in pre-concentration systems are in the fitting connections and valves.  Even so-called “zero dead volume” fittings have a gap between the tubing and the wall of the fitting where contamination can reside out of normal flow regions, especially when exposed to high VOC levels for an extended period of time.  The size of this un-swept volume is affected by how squarely cut and dressed the end of the tubing is that joins with the fitting and how far down in the compression fitting the tubing is seated.

Developed in the very early 1990’s, the configuration described is still the most used for the analysis of Hydrocarbons, Carbonyls and both TO-14 and TO-15.  Other, even more, advanced multistage trapping systems have been developed by Entech for headspace analysis and include the addition of Semi-Volatile Organic Compounds (SVOCs), Siloxanes, and Sulfur compounds.

7200 Preconcentrator

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The 7200 takes the industry standard, 7100A’s 3-stage preconcentration and water management technology, and elevates it to a whole new level. Many of the past limitations often seen in rotary valve based devices are now eliminated by combining digital valve isolation control with advanced robotic autosamplers, dropping the potential for carryover and cross-contamination far below previously obtainable levels.