Jörg Flock - X-Ray Fluorescence Spectroscopy for Laboratory Applications

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Provides comprehensive coverage 
on using X-ray fluorescence for laboratory applications
This book focuses on the practical aspects of X-ray fluorescence (XRF) spectroscopy and discusses the requirements for a successful sample analysis, such as sample preparation, measurement techniques and calibration, as well as the quality of the analysis results. 
X-Ray Fluorescence Spectroscopy for Laboratory Applications 
X
An important resource for the analytical chemist, providing concrete guidelines and support for everyday analyses Focuses on daily laboratory work with commercially available devices Offers a unique compilation of knowledge and best practices from equipment manufacturers and users Covers the entire work process: sample preparation, the actual measurement, data processing, assessment of uncertainty, and accuracy of the obtained results 
appeals to analytical chemists, analytical laboratories, materials scientists, environmental chemists, chemical engineers, biotechnologists, and pharma engineers.

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Finally, before using the test method it can be essential to validate the entire analytical process. According to ISO EN DIN 17025 (DIN-EN-ISO-17025 2005) the validation is defined as “ the confirmation by examining and providing proof that the special requirements for a specific intended use are met .” For that purpose, the required statistical parameters can be determined with the help of suitable reference samples or by comparing the analyses results of different samples with those of other independent analytical methods. These include the validity range of the method, and parameters such as trueness, repeatability and comparability, specificity and selectivity, as well as in the case of the detection of low mass fractions, the detection and determination limits. Validation is necessary to demonstrate the quality of an analytical method and to determine the achievable uncertainty of the analytical results.

2.4.2.5 Creation of an Analysis Report

Often, in addition to the analysis, a report must be prepared about all procedures and results of the analysis. It should include

the analytical instrument and measuring conditions used

the results of the individual measurements

the description of the evaluation method of the measurement results and a result summary

the discussion and estimation of possible errors in order to understand the contribution of every step of the analysis to the analytical uncertainties.

3 Sample Preparation

3.1 Objectives of Sample Preparation

It is generally assumed that the effort for sample preparation for X-ray spectrometry is very small, in particular since very different sample qualities can be analyzed and therefore, as with other analytical methods, the transfer of the starting material into a specific aggregate state is not necessary. Another common fact is that the sample is not modified by X-ray fluorescence (XRF). This is only true, however, insofar as the sample, which is used for measurement in the instrument, will not be changed and will be consequently available for further analytical procedures. Yet, significant changes to the sample material may be required during the preparation procedure itself.

The types of materials that can be analyzed by X-ray spectrometry range from compact homogeneous solids to small samples and liquids, as well as nonhomogeneous samples. Careful preparation of these different materials is the prerequisite for correct analytical results. With the sample preparation, different goals are pursued:

At first, the sample must be adapted geometrically to the instrument. For this purpose, it may be necessary to cut samples to size or prepare them such that they can be positioned in the measuring instrument, for example, cutting disks from the material, pressing powder samples into tablets, or filling fluids into suitable measuring cells.

On the other hand, the result of the sample preparation must be a laboratory sample for which the analyzed volume corresponds to the material to be characterized and for which the surface texture does not influence the measurement result. Owing to the limited penetration depth of X-rays, in particular for light elements, this means that in the case of solid-state samples, the surface must be free of corrosion layers. In addition, the surface roughness should be less than the information depth of the fluorescence radiation with the lowest energy emanating from the sample, or in the case of powder samples, the grain sizes should be of the same order of magnitude as the information depth.

An important objective of sample preparation can be the production of a homogeneous sample in order to reduce the influence of mineralogical effects, and the influence of matrices or surface roughness. In this way, the analytical accuracy can be influenced by the different preparation methods.

The sample composition should not change during analysis, i.e. both chemical reactions and influences by the excitation radiation are to be avoided by suitable preparation as far as possible. However, it is also possible to make selective changes to the sample type in order to prepare them for measurement. In this case, however, a determination of the recovery rates through intensive studies is recommended.

Different preparation methods are available for the various sample qualities – they are used depending on the desired analytical accuracy as well as the time available for the analysis. In this chapter, we will give examples of the commonly used preparation techniques for different sample qualities including their time and effort, but also with their effect on the achievable analytical accuracies. Where applicable, more detailed descriptions of the preparation techniques are discussed in connection with the presentation of individual analytical tasks.

Problems of sampling are not covered here since they are very much dependent on the respective analytical questions. It is assumed that the material to be examined is already available and has been processed by the initial preparation steps, e.g. crushing and, if applicable, multiple milling and separation. It is available not only in sufficient quantity, but also in quality that adequately represents the material to be investigated.

The samples produced prior to preparation as well as those produced by the preparation are named differently according to their state and their intended purpose according to DIN 51418-2 (DIN-51418-2 2014). The material that is provided for analysis is called a laboratory sample. This sample can be analyzed either with or without further preparation.

The measuring sample is the sample measured with the analyzer; the retained sample is the sample that is archived for necessary traceability. It can be either the measuring sample itself or a sample prepared in parallel. The measuring samples are distinguished according to their purpose; there are analyte samples, calibration samples, recalibration samples, drift correction samples, blank samples, and others.

3.2 Preparation Techniques

3.2.1 Preparation Techniques for Solid Samples

The variety of solid samples is very large. This results in a corresponding high number of different preparation techniques. Caused by the large influence of sample preparation to the analytical result not only the measurement methods but also the preparation techniques for special sample qualities are standardized. Table 3.1summarizes the typical preparation techniques for the most common sample types.

3.2.2 Information Depth and Analyzed Volume

The information depth is an important parameter for the assessment of sample preparation. It depends on the energy of the fluorescence radiation of the elements of interest as well as on the matrix of the sample. In the case of XRF, the incident radiation penetrates into the material, is absorbed on its way through the sample, and thereby generates fluorescent radiation. The radiation must reach the sample surface in order to be detected by the spectrometer. On its way, the fluorescence radiation is attenuated, i.e. only the radiation from a well-defined sample layer reaches the sample surface. This is referred to as the information depth.

Table 3.1 Preparation technologies for solid samples.

Sample type Compact and homogeneous Compact and inhomogeneous Powder-like Liquid
Example Metals, glasses Minerals (ores, rocks, etc.), glasses, metal alloys, metal swarfs Minerals (ores, slags, soil, sludge, etc.) powder, dust Solutions, melts
Homogenization Usually not necessary, where appropriate remelting Metals , glasses : remelting ⟹ transfer into compact homogeneous material (from here see compact and homogeneous) Minerals : crushing, grinding ⟹ transfer into powder-like material or direct analysis ⟹ position-sensitive analysis (see Chapter 13) Grinding, digestion, melting, solution Stirring, shaking, where appropriate, filtering of solid components (as powder-like material)
Shaping Sawing, cutting, turning, drilling, milling Pouring of the powder in sample cups, pressing of disks, preparation of melted disks Pouring in sample cups
Surface preparation Polishing or milling with a roughness adapted to the elements to be analyzed Realized with shaping Given by covering of the sample cup
Figure 31 Information depth of fluorescence radiation Because the energy of - фото 24

Figure 3.1 Information depth of fluorescence radiation.

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