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Procedure - Solid Samples

Instrument calibration/drift correction.

Place the calibration/drift standard in a *** Nickel Basket, and if applicable, place the sample into the appropriate autoloader position.

Press the Analyze button on the instrument screen. After a short delay, the loading head slide-block will open.

Note: samples using automation should be placed in the appropriate autoloader position before starting the

analysis sequence. Once the sequence has started, the automatic analysis will start and end automatically.

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Instrument Highlights and Features

Features and Benefits

LED light ring illuminates the furnace area

Choice of either argon or helium carrier gas

Novel electrode design increases heat transfer efficiency for increased stability

Non-touch interface systems are also available

User-friendly brand software

High-Performance Detector Design

Thermostatic construction provides increased protection from ambient temperature fluctuations

Optimized emitter control and detection circuitryimproves the IR cell lifetime and long-term stability,

resulting in superior accuracy and precision

Infrared detection for the determination of oxygen, thermoconductivity detection for the determination

of nitrogen

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Sample Preparation

Typically, titanium and zirconium samples are chemically etched to remove surface contamination when oxygen and nitrogen are determined. However, etching can introduce hydrogen into the sample.

ASTM method E 1409 "Determination of Oxygen and Nitrogen in Titanium and Titanium Alloys by the Inert

Gas Fusion Technique", as updated in 1996, permits either etching or abrading (filing) of the test specimen.

ASTM E 1447 "Determination of Hydrogen in Titanium and Titanium Alloys by the Inert Gas Fusion Thermal

Conductivity/Infrared Detection Method" permits surface preparation by abrading (if necessary to remove

contamination). Differences in sample preparation present somewhat of a dilemma regarding simultaneous

determination of O, N, and H in titanium. However, abrading samples with a file to remove surface

contamination will yield accurate O, N, and H results. The ONH836 utilizes a high-power electrode furnace to quickly and efficiently release the target gases from within the sample, which allows for a very rapid simultaneous determination of oxygen, nitrogen, and hydrogen.

ONH836仪器通过***采纳客户的反馈意见和创新设计。

Procedure – Powder/Chip Samples

Determine the instrument blank.

Press the Analyze button on the instrument screen again, the loading head slide-block will close and the lower electrode will open.

Clean the upper and lower electrode either manually or remove the crucible and press the analyze button to clean with an automatic cleaner if applicable.

Add approximately 0.05 g of *** Graphite Powder to a 782-720 Graphite Crucible.

Firmly place the crucible on the lower electrode tip or appropriate autoloader position.

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Method Selection

Two methods are described in this application note; either method can be used to analyze iron, steel, nickel-, and cobalt-base alloys. The Precision Method is recommended for general use and will provide the best precision and accuracy throughout the typical O, N, and H concentrations found in this group of metals; approximate cycle time is 3.5 minutes. The Fast Track method can be used where speed of analysis is a critical component; for example, when molten metal is being sampled and results are required in the shortest possible time. This method will produce suitable results for most samples; approximate cycle time is 2.25 minutes. As noted above, sampling and sample preparation are key elements to accurate O, N, and Hdetermination as well. It is up to the user to determine which method best meets their needs.

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