Agilent 720-ES Axial ICP-OES Mercury Determination Application Note

This paper describes a method for on-line addition of stannous chloride for determination of mercury by ICP-OES. This method allows mercury detection from µg/L to μg/L.


Agilent 720-ES Axial ICP-OES Mercury Determination Application Note - cover page
Brand
Agilent
Category
Other Electronics
Document type
Application Note
Language
English
Pages
4
File format
PDF
File size
131 KB
Published
12 June, 2012
Updated
01 October, 2023
Model
720-ES
MD5 checksum
B449D1E886551A2CDADC6DA1437F7E94

About this manual

This document details a method for determining mercury (Hg) in various water types and wastes using an Agilent 720-ES axially-viewing Inductively Coupled Plasma-Optical Emission Spectrometer (ICP-OES). The method employs on-line addition of stannous chloride (SnCl2) as a reducing agent to enhance the Hg signal, allowing for detection in the pg/L range without requiring a dedicated cold vapor generation accessory like the VGA-77.

The text outlines the instrumentation setup, including the use of a four-channel peristaltic pump and a Y-piece to combine sample and reductant flows. It provides specific operating parameters, sample preparation instructions for NIST 1641D reference material, and discusses the results of signal enhancement and detection limits achieved with this technique.

What's inside

  • Introduction
  • Instrumentation
  • Materials and Reagents
  • Sample Preparation
  • Results and Discussion
  • Detection Limit
  • Analysis of NIST 1641D
  • Conclusion

Specifications

Power1.2 kW
Plasma gas flow15 L/min
Auxiliary gas flow1.5 L/min
Nebulizer flow0.65 L/min
Pump speed12 rpm
Sample uptake rate1.0 mL/min
Replicate read time30s
Sample uptake delay time80s
Rinse time120s

Frequently asked questions

How should the torch be cleaned after analysis?

Soak the torch in concentrated HCl to dissolve the white SnO2 deposit, then rinse with de-ionized water and dry.

What is the recommended procedure for cleaning white powder deposits from the end of the torch after analysis?

To remove the deposit, soak the torch directly in concentrated HCl to dissolve it, then rinse with de-ionized water and allow it to dry.

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