Natural reference material

Other procedures for the evaluation of disintegration during composting in full-scale testing have been discussed in which the sample is introduced in net bags into a composting pile. However, national or international standards have not been published yet. In addition, for disintegration it is important to validate test procedures by the use of (natural) reference materials. 

For example, if a carbonaceous sample (S) is examined mass spectrometrically, the ratio of abundances for the carbon isotopes C, in the sample is Rg. This ratio by itself is of little significance and needs to be related to a reference standard of some sort. The same isotope ratio measured for a reference sample is then R. The reference ratio also serves to check the performance of the mass spectrometer. If two ratios are measured, it is natural to assess them against each other as, for example, the sample versus the reference material. This assessment is defined by another ratio, a (the fractionation factor Figure 48.2). 

An additional complication is that most dynamic data are stated for configurations involving reference materials such as water, air, and so on. The nature of the process material will affect the dynamic characteristics. For example, a thermowell will exhibit different characteristics when immersed in a viscous organic emulsion than when immersed in water. It is often difficult to extrapolate the available data to process conditions of interest. 

Laser based mass spectrometric methods, such as laser ionization (LIMS) and laser ablation in combination with inductively coupled plasma mass spectrometry (LA-ICP-MS) are powerful analytical techniques for survey analysis of solid substances. To realize the analytical performances methods for the direct trace analysis of synthetic and natural crystals modification of a traditional analytical technique was necessary and suitable standard reference materials (SRM) were required. Recent developments allowed extending the range of analytical applications of LIMS and LA-ICP-MS will be presented and discussed. For example ... 

The set of Glass Standard Reference Material NIST SRM 610 - 614 was used for quantification of amount up to 45 trace elements in the synthetic oxide single crystals and natural quartzites. 

When this is done it is seen that in all cases plastics materials, before compounding with additives, consist of a mass of very large molecules. In the case of a few naturally occurring materials, such as bitumen, shellac and amber, the compositions are heterogeneous and complex but in all other cases the plastics materials belong to a chemical family referred to as high polymers. 

Because of the complex nature of the discharge conditions, GD-OES is a comparative analytical method and standard reference materials must be used to establish a unique relationship between the measured line intensities and the elemental concentration. In quantitative bulk analysis, which has been developed to very high standards, calibration is performed with a set of calibration samples of composition similar to the unknown samples. Normally, a major element is used as reference and the internal standard method is applied. This approach is not generally applicable in depth-profile analysis, because the different layers encountered in a depth profile of ten comprise widely different types of material which means that a common reference element is not available. 

Standardization. Standardization in analytical chemistry, in which standards are used to relate the instrument signal to compound concentration, is the critical function for determining the relative concentrations of species In a wide variety of matrices. Environmental Standard Reference Materials (SRM s) have been developed for various polynuclear aromatic hydrocarbons (PAH s). Information on SRM s can be obtained from the Office of Standard Reference Materials, National Bureau of Standards, Gaithersburg, MD 20899. Summarized in Table VII, these SRM s range from "pure compounds" in aqueous and organic solvents to "natural" matrices such as shale oil and urban and diesel particulate materials. 

Another issue in the preparation of reference material is the required shelf life. The shelf life of reference material is the time that it remains stable under proper storage conditions. Depending on the nature of the mechanisms affecting the stability of the material, various actions can be taken to improve the shelf life. Reduction of the moisture content is one of the first options to be considered. In many cases, moisture plays a key role in mechanisms leading to instability of the matrix and/or parameters. In other cases, sterilization or pasteurization of the material might be considered in order to stop bacterial activity. When preparing solutions, additives may increase the shelf life. Obviously, the shelf life of material is also a function of the storage conditions. 

Bowman WS (1994) Stream sediment reference materials STSD-i to STSD-4. In Catalogue of Certified Reference Materials, CCRMP 94-iE. Natural Resources Canada, Ottawa. 

Certified reference materials (CRMs) to validate measurements of organic constituents were introduced in the early 1980 s, more than a decade after the development of the first natural matrix CRMs for inorganic constituents. There are three types of CRMs to support measurements of organic constituents ... 

Leaver ME, and Bowman WS (1994b) CCRMP s Custom Reference Material Preparation Service. Mineral Sciences Laboratories Division Report MSL 94-42 (OP J) Draft. CANMET, Natural Resources Canada, Ottawa. Proceedings of the 1994 Joint Conference of the Sodety of Mineral Analysts and the Canadian Mineral Analysts, pp 247-256. Winnemucca, NV, 1994 April 18-22. 

Some of the intended categories of use of radioisotopic reference material have been reviewed recently by Fajgelj et al. (1999). They include assignment of property values, establishing the traceability of a measurement result, determining the uncertainty of a measurement result, calibration of an apparatus, assessment of a measurement method, use for recovery studies and use for quality control purposes. It should be noted however that, in general, natural matrix reference materials are not recommended for calibration purposes. This should preferably be done with pure chemical forms of the element labelled with the isotope of interest. Calibrated isotopic sources of this kind are available from a number of commercial suppliers and are not the subject of this review. 

A wide variety of reference materials is now available, covering several different kinds of natural matrix such as food (e.g. milk powder), human tissues (e.g. liver), marine biological materials (e.g. tuna fish) and soils and sediments. The radionuclides of interest cover naturally occurring ones (e.g. Ra), fission products... 

The concept of preparing a reference material with property values traceable to SI units is a relatively recent one which has not yet been applied in practice to natural matrix radioisotopic reference materials. This is one of the main reasons why such materials are generally not recommended for calibration purposes. 

Zeisler R (2000a) Investigations by INAA for the Development of Natural Matrix Standard Reference Materials (SRMs) Suitable for Small Sample Analysis. J Radioanal Nucl Chem 245 73-80. 

The development of G-i and W-i (Ahrens 1951 Fairbairn et al.1951 Stevens et al. i960) was the response to this demand with respect to dc arc emission spectrogra-phy. As similar samples are used routinely in calibration for XRF and INAA analyses, many geological samples have been developed as reference materials since that time to support geoanalysis (Potts et al.1992). Just as the change from classical to instmmental methods of analysis changed the nature of demands for reference... 

The revised database holds over 23 000 analyte values for 660 measurands and 1670 reference materials produced by 56 different producers, from 22 countries. The database is restricted to natural matrix materials (i.e. made from naturally occurring materials, excluding calibration standards manufactured from pure chemicals). Information has been extracted from the relevant certificates of analysis, information sheets, and other reports provided by the reference material producers. As a general rule, the authors have only included in the compilation reference materials for which a certificate of analysis or similar documentation is on file. Information included in the survey is on values for measurands determined in reference materials, producers, suppliers, the cost of the materials, the unit size supplied, and the recommended minimum weight of material for analysis, if available. The new searchable database has been designed to help analysts to select reference materials for quality assurance purposes that match as closely as possible, with respect to matrix type and concentrations of the measurands of interest and their samples to be analyzed see Table 8.3. 

The Babylonians and Assyrians cemented stone slabs as well as bricks with bitumen (which is sometimes also referred to as asphalt), a mixture of a black or brown natural organic material with a pitchy luster and comminuted mineral. Bitumen is a thermoplastic solid material when heated above 50°C, it softens and becomes a thick, viscous liquid that reverts to a solid on cooling. It is composed of a natural mixture of hydrocarbons (organic substances composed of carbon, hydrogen, and oxygen) that occurs in natural... 

Elaboration of the method for the identification of colour compounds by RPLC MS should comprise four steps (1) spectral characterization of reference materials (standards) and subsequent optimization of detection parameters, as well as those of their chromatographic separation (2) analysis of natural dyestuffs used as colouring materials in historical objects (3) analysis of model samples (dyed fibres, paintings) prepared according to old recipes (4) application of the acquired knowledge to identification of colourants present in historical objects. 

Gill and Fitzgerald [481] determined picomolar quantities of mercury in seawater using stannous chloride reduction and two-stage amalgamation with gas-phase detection. The gas flow system used two gold-coated bead columns (the collection and the analytical columns) to transfer mercury into the gas cell of an atomic absorption spectrometer. By careful control and estimation of the blank, a detection limit of 0.21 pM was achieved using 21 of seawater. The accuracy and precision of this method were checked by comparison with aqueous laboratory and National Bureau of Standards (NBS) reference materials spiked into acidified natural water samples at picomolar levels. Further studies showed that at least 88% of mercury in open ocean and coastal seawater consisted of labile species which could be reduced by stannous chloride under acidic conditions. 

Reagent Purity The purity of many reagents is specified by the manufacturer as being not less than a specified value. Any assumptions about the degree of purity will contribute to the uncertainty. The nature of any impurities may also be important. Pure substance Certified Reference Materials will have a stated purity, plus an estimate of the uncertainty associated with the purity value. 

These are flavours that are produced synthetically but are not present in a natural flavouring material. The chemistry of flavours is a complex topic that has been the subject of many books, for example ref. 3. Synthetic flavours are made from a mix of flavouring substances that have been found to produce a given flavour note . Those who develop flavours are referred to as flavourists. Flavourists take the musical analogy of notes further by referring to the top notes and the bottom notes of a flavour. 

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