A COMPREHENSIVE STABILITY STUDY ON THE XPLORER TOTAL SULFUR/TOTAL NITROGEN ANALYZERS
An elemental combustion analyzer is able to measure the amount of Total Nitrogen, and Total Sulfur by means of high- temperature combustion (approximately 1000 ˚C) in an oxygen-rich environment. In Trace Elemental combustion elements can be detected from trace level (µg/kg/ ppb level) up to 10.000 ppm/ mg/L (1%) there where the elemental analyzers for CHNSO are mainly designed for a high-level percentage measuring range.
By combusting sample material (Solid, Liquid or Gas), NO and SO2 are formed which can be detected by a Pulsed UV-Fluorescence
followed by a Chemiluminescence detector.
Our quartz combustion tube is constructed in such a way that it allows direct injection of the sample into the heated oxidation zone of the furnace and/or to accommodate the sample introduction using a quartz sample boat. The surface of the oxidation section of the combustion tube must be large enough to ensure complete oxidation of the sample. However, some elemental combustion analyzer manufacturers pack the quartz combustion tube with an oxidation catalyst to achieve this.
The XPLORER Series does not make use of oxidation catalyst: The unique construction of the Xplorer combustion tubes is designed in such a way, to always deliver suffi cient oxidation power on samples that are diffi cult to combust.
More recently, ceramic material has been introduced as an alternative to fully quartz combustion tubes, for better protection of the tube when running samples containing high halogen concentrations (or other components which might attack the quartz material).
Detection of Total Nitrogen – Chemiluminescence
When Nitrogen components are combusted in the high- temperature furnace, the following reaction takes place:
R - N+ O2 NO + H2 O + CO2
After complete sample oxidation, the combustion gas is conditioned by removing water vapor and particles.
Ozone is added to the conditioned gas stream in the Chemiluminescence reaction chamber. Ozone reacts with Nitric Oxide (NO) to form Nitrogen Dioxide in an excited state (NO2
*).
The emitted light is detected by a Photomultiplier Tube (PMT). The amount of detected emitted light corresponds with the amount of NO (Total Nitrogen) present in the sample.
Detection: NO + O3
NO2 * NO2 NO2 * + O2 + hv1
Detection of Total Sulfur – UV-Fluorescence
When organic Sulfur components are combusted in the high- temperature furnace, the following reaction takes place:
R-S + O2 → SO2 + H2 O + CO2
After complete sample oxidation, the combustion gas is conditioned by removing water vapor and particles.
The conditioned gas stream containing the Sulfur Dioxide (SO2 at specifi c wavelengths and due to the unstable character of
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molecules is transferred to the reaction chamber. The Xenon fl ashed UV lamp will excite the Sulfur Dioxide molecules to SO2
* the SO2
Xplorer TN/TS with Archie autosampler * it will relax back to SO2 instantly. The released energy
will be emitted in the form of light and will be detected by the Photomultiplier Tube (PMT). The amount of light emitted equals the total amount of SO2
(Total Sulfur) present in the sample.
Detection: SO2
SO2
+ hv1 → SO2 * → SO2
* + hv2 Stability study setup
The following Xplorer elemental combustion analyzers have been used to perform the analysis of Total Nitrogen (CLD) and Total Sulfur (UV-F):
- Xplorer TN/TS - Xplorer-V TN/TS
Horizontal furnace based setup Vertical furnace based setup
All samples were introduced by direct liquid injection with either the Archie autosampler (combined with Horizontal Xplorer TN/ TS) or the integrated liquid autosampler of the Xplorer-V. Basic standard method parameters were applied to the 3 sample matrices (see systems settings below). The samples were analyzed daily on the two systems for the duration of three months.
No calibration or re-calibration was applied to the setup during the 3 months stability study. Other than small minor maintenance tasks (replacing needles, replacing septum or refi lling of solvents) no intervention was allowed to check potential drift or stability issues on the furnace, detectors and complete analyzer setup.
Xplorer-V NS
Sample Information Sample Type Component
Methods Applicable*
*instrumentation complies with
mentioned norms but is not limited by them
Diesel, Petrol, Xylene based CRM Standards Nitrogen, Sulfur
Concentration 0.1 – 100 mg/l
ASTM D5453 ASTM D6667 ASTM D7183 EN 20846
ASTM D4629 ASTM D5762 ASTM D6069 ASTM D7184
Summary
During a run time of 3 months, both analyzers showed excellent stability over the complete course. As mentioned, only minor maintenance actions were allowed (e.g. needle changes, septa and fi lters) both systems were running on their initial calibration lines during the course of the test.
For the evaluation of the data, Tier 3 regulations for the calculation of system stability were applied to all the results, more information can be found in ASTM 7039. In the document, an R factor is calculated according to systematic standard deviation and averages, which results in maximal allowed limits for both accuracy and precision.
See section “results” for more in-depth information concerning the outcome of the study.
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