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1.
The International Measurement Evaluation Programme (IMEP) attempts to shed light on the current state of the practice in
chemical measurements. The main tool, which assists this attempt and also differentiates IMEP from similar projects, is the
establishment of SI-traceable reference ranges (where possible) for the elements offered for measurement to the participants
for every IMEP round. The Institute for Reference Materials and Measurements (IRMM), as the founder and co-ordinator of IMEP
has the responsibility of establishing the SI-traceable reference ranges. This is a large task that requires knowledge, skill
and resources. IRMM collaborates with a network of reference laboratories in order to achieve the establishment of SI-traceable
reference ranges in a transparent and reliable way. The IMEP reference laboratories must have demonstrated experience and
have a proven and successful record in the use of primary methods of measurements (mainly isotope dilution mass spectrometry)
and the application of uncertainty evaluation according to ISO/BIPM guidelines. In IMEP-9 "trace elements in water", results
from 7 reference laboratories (including IRMM) were combined by IRMM to establish SI-traceable ranges for the 15 elements,
which were then offered for measurement to the 200 participants worldwide. This paper does not discuss the individual contribution
of the reference laboratories (this could be the subject of individual papers) but describes the procedures and criteria used
in order to establish the reference ranges for the IMEP-9 samples by combining the individual contributions. All results submitted
to IRMM are included, so as to make this publication as realistic as possible.
Received: 31 December 1999 / Accepted: 7 March 2000 相似文献
2.
I. Kuselman Alexander Weisman Wolfhard Wegscheider 《Accreditation and quality assurance》2002,7(3):122-124
The traceability of in-house reference materials (IHRM) is discussed. It is shown that a systematic error in results of a
measured value, specific to a measurement method or to a laboratory developing an IHRM, can be overcome if a comparative approach
to IHRM characterization is used. A traceability chain of the value carried by the IHRM to the value carried by the reference
material with higher metrological status and sufficiently similar matrix (for example, a certified reference material – CRM
according to ISO Guide 30) is helpful in such a case. The chain is realized when the IHRM samples are analysed simultaneously
with the CRM samples under the same conditions. This and other traceability chains necessary for the IHRM development are
examined as the measurement information sources. 相似文献
3.
J. Vogl D. Liesegang M. Ostermann J. Diemer M. Berglund C. R. Quétel P. D. P. Taylor K. G. Heumann 《Accreditation and quality assurance》2000,5(8):314-324
The present paper describes the certification of the amount content of Cd, Cr and Pb in two different polyethylene materials
within the third phase of the Polyethylene Elemental Reference Material (PERM) project. The analytical procedure to establish
the reference values for Cd, Cr and Pb amount contents in these materials is based on isotope dilution mass spectrometry used
as a primary method of measurement. Cd and Pb were measured with inductively coupled plasma-mass spectrometry and Cr with
positive thermal ionization-mass spectrometry. The decomposition of the polymer matrix was carried out using a high pressure
asher. Reference values for amount content, traceable to the SI-system, have been obtained for these three elements in both
of the polyethylene samples of PERM. For each of the certified amount content values an uncertainty budget was calculated
using the method of propagation of uncertainties according to ISO and EURACHEM guidelines. The measurement procedures, as
well as the uncertainty calculations, are described for all three elements. In order to keep the whole certification process
as transparent as possible, the preparations of various reagents and materials as well as the sample treatment and blending
are described in detail. The mass spectrometry measurements and the data treatment are also explained carefully. The various
sources of uncertainty present in the procedure are displayed in the uncertainty budgets. The obtained combined uncertainties
for the amount content values were less than 2% relative (k=1) for all investigated elements. The amount contents were in
the μmol/kg range, corresponding to mg/kg levels.
Received: 21 October 1999 / Accepted: 29 January 2000 相似文献
4.
A method is suggested for the calculation of a reference value and its uncertainty to be used in the frame of an interlaboratory
comparison (ILC). It is assumed that the reference value of the measurand is determined independently from the ILC round.
It is derived from a limited set of measurement results obtained from one or several expert laboratories. The procedure involves
three stages: (1) check of the experimental data and possible corrections; (2) check of the consistency of data, and possibly
increase of the uncertainties in order to attain internal consistency; (3) choice between fully, partially or un-weighted
mean. 相似文献
5.
The International Measurement Evaluation Programme (IMEP) is an interlaboratory comparison scheme founded, owned and co-ordinated by the Institute for Reference Materials and Measurements (IRMM) since 1988. IMEP-14, for the first time in the series, is focusing on trace elements in sediment. Reference values for ten elements stating total concentrations and expanded uncertainties according to GUM were established. In total, 239 laboratories from 43 countries in five continents participated in the comparison, and the degree of equivalence between the results from the laboratories and the reference values is presented graphically. Identical samples were distributed to nine National Measurement Institutes within the frame of the CCQM-P15 pilot study. Participation in the IMEP-14 interlaboratory comparison was offered to laboratories in the EU new member states and acceding countries according to the IRMMs Metrology in Chemistry support programme for EU new member states and acceding countries.This revised version was published online in August 2004 with corrections to text especially to the Discussion section. 相似文献
6.
Ines BaerJohannes van de Kreeke Thomas Peter Josef LinsingerPiotr Robouch Fernando Cordeiro RaposoBeatriz de la Calle 《Trends in analytical chemistry : TRAC》2011,30(2):313-323
The International Measurement Evaluation Program (IMEP) organized the IMEP-24 interlaboratory comparison after reports in the media about high levels of lead in toys. The aim of this comparison was to verify the laboratories’ capacity to evaluate trace-element levels in a possible toy-like material according to the European Standard EN 71-3:1994. As test material, it used a former certified reference material containing levels of antimony, arsenic, barium, cadmium, chromium, mercury, lead and selenium around the limits set in the standard.Four expert laboratories confirmed the reference values (Xref) for all elements but Hg, and established a reference value for Hg. The scatter of the results reported by the participants was large, as expected, but showed a close to normal distribution around the reference values for five of the eight trace elements. The spread of results was mainly attributed to sampling and sample preparation.One major issue observed in this exercise was the lack of legislative rules about how to report the result, or, more specifically, the use of the analytical correction, which was introduced in EN 71-3:1994 to achieve consistent interpretation of results and which is to be applied when values are equal to or above the maximum limits set in the standard. Its application by the participants was very inconsistent and led to problems in their evaluation. There is clearly a need for clarification and for more formal regulations with regard to result reporting in order to minimize the risk of confusion.Participants were also asked to give their opinion with regard to the acceptability of the test material for the market. The majority correctly considered the material as non-compliant. However, almost one-third incorrectly assessed the material as compliant. 相似文献
7.
Ines BaerJohannes van de Kreeke Thomas Peter Josef LinsingerPiotr Robouch Fernando Cordeiro RaposoBeatriz de la Calle 《Trends in analytical chemistry : TRAC》2011,30(7):1177
The International Measurement Evaluation Program (IMEP) organised the IMEP-24 interlaboratory comparison after reports in the media about high levels of lead in toys. The aim of this comparison was to verify the laboratories’ capacity to evaluate trace-element levels in a possible toy-like material according to the European Standard EN 71-3:1994. As test material, it used a former certified reference material containing levels of antimony, arsenic, barium, cadmium, chromium, mercury, lead and selenium around the limits set in the standard.Four expert laboratories confirmed the reference values (Xref) for all elements but Hg, and established a reference value for Hg. The scatter of the results reported by the participants was large, as expected, but showed a close to normal distribution around the reference values for five of the eight trace elements. The spread of results was mainly attributed to sampling and sample preparation.One major issue observed in this exercise was the lack of legislative rules about how to report the result, or, more specifically, the use of the analytical correction, which was introduced in EN 71-3:1994 to achieve consistent interpretation of results and which is to be applied when values are equal to or above the maximum limits set in the standard. Its application by the participants was very inconsistent and led to problems in their evaluation. There is clearly a need for clarification and for more formal regulations with regard to result reporting in order to minimise the risk of confusion.Participants were also asked to give their opinion with regard to the acceptability of the test material for the market. The majority correctly considered the material as non-compliant. However, almost one-third incorrectly assessed the material as compliant. 相似文献
8.
J. Vogl C. R. Quétel M. Ostermann I. Papadakis L. Van Nevel P. D. P. Taylor 《Accreditation and quality assurance》2000,5(7):272-279
The present paper describes the contribution of the Institute for Reference Materials and Measurements to the certification
of B, Cd, Mg, Pb, Rb, Sr, and U amount contents in a natural water sample, in round 9 of the International Measurement Evaluation
Programme (IMEP-9). The analytical procedure to establish the reference values for B, Cd, Mg, Pb, Rb, Sr, and U amount contents
was based on isotope dilution inductively coupled plasma-mass spectrometry used as a primary method of measurement. Applying
this procedure reference values, traceable to the SI, were obtained for the natural water sample of IMEP-9. For each of the
certified amount contents presented here a total uncertainty budget was calculated using the method of propagation of uncertainties
according to ISO and EURACHEM guidelines. The measurement procedures, as well as the uncertainty calculations are described
for all seven elements mentioned above. In order to keep the whole certification process transparent and so traceable, the
preparations of various reagents and materials as well as the sample treatment and blending, the measurements themselves,
and finally the data treatment are described in detail. Explanations focus on Pb as a representative example. The total uncertainties
(relative) obtained were less than 2% for all investigated elements at amount contents in the pmol/kg up to the high μmol/kg
range, corresponding to low μg/kg and mg/kg levels.
Received: 21 October 1999 / Accepted: 29 January 2000 相似文献
9.
A.M.H. van der Veen 《Accreditation and quality assurance》2002,7(1):2-6
The availability of certified reference materials, certified in accordance to the GUM is an important tool for the proper
estimation of measurement uncertainty in routine analysis. Many CRMs may suffer from incomplete or wrongly estimated uncertainties,
mainly due to lack of guidance on how to implement the GUM in the production of CRMs. In particular the inclusion of the impact
of inhomogeneity and instability in the uncertainty budget is often missing. The ongoing revision of ISO Guide 35 aims to
fill this gap in providing guidance how (batch) inhomogeneity and instability can be translated into measurement uncertainty.
The structure of the current ISO Guide 35 has been maintained as far as possible, but major parts underwent revision to become
better aligned with GUM and ISO Guide 34 (2000).
Received: 9 April 2001 Accepted: 22 October 2001 相似文献
10.
The present situation of Japanese certified reference materials registered in the COMAR database 总被引:1,自引:0,他引:1
In the field of reference materials, COMAR (Code d'Indexation des Matériaux de Référence) is now internationally known as
a reliable directory. In order to improve the quality of COMAR, a document which covers general requirements for the registration
of reference material has recently been adopted by the Japanese coding centre, NITE. This paper describes the general requirements
for reference materials and the current status of the COMAR database coded by the National Institute of Technology and Evaluation
(NITE), Japan. The concept of the requirements is fundamentally based on the ISO Guides 30, 31, 33, 34 and 35. Certifications
of reference materials are divided into the following three categories in the newly adopted document.
1. Certifications based on the results of interlaboratory comparisons
2. Certifications in accordance with the Measurement Law
3. Certifications in accordance with the measurement results of national institutions
An example of an uncertainty evaluation is also presented in the paper.
Received: 14 October 1996 Accepted: 3 December 1996 相似文献
11.
The preparation and analysis of the oxygen mass fraction of three pure copper reference materials (BAM-379/1, BAM-379/2, BAM-379/3)
intended for the calibration of spark emission spectrometry are described here. Data of homogeneity testing and round robin
certification in collaboration with 12 independent laboratories from metalworking industry and research are reported. Problems
with the establishment of traceability in this special case are discussed.
Received: 20 July 2001 Accepted: 13 October 2001 相似文献
12.
Ioannis Papadakis Lutgart Van Nevel Caroline Harper Yetunde Aregbe Philip D. P. Taylor 《Accreditation and quality assurance》2007,12(2):105-111
The International Measurement Evaluation Programme (IMEP) is an interlaboratory comparison scheme, founded, owned and co-ordinated
by the Institute for Reference Materials and Measurements (IRMM) since 1988. IMEP-12, for the fourth time in the series, focused
on trace elements in water and it was designed specifically to support European Commission directive 98/83/EC. Reference values
for the concentration of ten elements were established with expanded uncertainties according to GUM. In total, 348 laboratories
from 46 countries in five continents participated in the comparison and the degree of equivalence between the results of the
laboratories and the reference values is presented graphically. Samples from the same batch were distributed to ten laboratories
from European Countries, which represented their country in the framework of the EUROMET project 528. Participation in this
comparison was offered to the European Co-operation for Accreditation (EA) for participation of accredited laboratories from
all over Europe in the framework of the collaboration between IRMM and EA and to laboratories from the EU new member states
and acceding countries in the frame of IRMM’s ‘Metrology in Chemistry support program for EU new member states and acceding
countries.’ 相似文献
13.
Ian Robert Juniper 《Accreditation and quality assurance》1998,3(2):79-82
Certified reference materials are widely used for the calibration of measuring equipment and for the evaluation or validation
of measurement procedures. The use of reference materials makes possible the transfer of the values of measured or assigned
quantities between testing, analytical and measurement laboratories, both nationally and internationally. There is an increasing
number of reference materials producers in other countries, and a demonstration of their scientific and technical competence
is now more widely considered to be a basic requirement for ensuring the quality of reference materials. This article outlines
recent activities by international bodies and their culmination in a scheme of accreditation of certifiers of reference materials
which has been developed by the National Association of Testing Authorities, Australia (NATA). 相似文献
14.
P. De Bièvre 《Accreditation and quality assurance》2000,5(6):224-230
Traceability is a property of the result of a measurement. Since values carried by (reference) materials must also have been
obtained, of necessity, by measurement, the definition of traceability also applies to reference materials. It is extremely
helpful to give the traceability (of the origin) of a reference material a separate name, i.e. 'trackability'. An analysis
of the function of values carried by reference materials, shows that they can fulfill different functions, depending on the
intended use. One of the functions located outside the traceability chain – and hence not very relevant for establishing traceability
– is evaluating the approximate size of the uncertainty of the measurement of an unknown sample by performing a similar measurement
on a reference material, used as a 'simulated sample'. Another function is located inside the traceability chain, where the
reference material is used as an added 'internal standard'. Then, the value carried by the reference material is essential
for establishing the traceability of the measured value of an unknown sample. In the latter application, the reference material
acts as an 'amount standard' (the certified value for amount is used).
Received: 11 November 1999 / Accepted: 24 February 2000 相似文献
15.
I. Šperlingová L. Dabrowská V. Stránský J. Kuˇcera M. Tichý 《Accreditation and quality assurance》2003,8(3-4):113-116
A preliminary batch of the reference material was prepared by freeze-drying pooled urine samples obtained from healthy persons
occupationally exposed to styrene. Tests for homogeneity and stability were performed by determining urine concentrations
of mandelic (MA) and phenylglyoxylic acids (PGA). The urinary MA and PGA concentrations were followed over an 8-month period
using high performance liquid chromatography (HPLC). No changes of the concentration values were found. Pure PA and PGA from
Merck and Fluka, respectively, were used for traceability purposes, because certified or standard reference materials for
MA and PGA do not exist. Control material ClinChek-Urine Control (Recipe) was analysed simultaneously. The mean values of
MA and PGA compared well with the means of control samples and fell within the control range. The certified values and their
uncertainties were evaluated from the results of interlaboratory comparisons, homogeneity (277.0 ± 7.4 mg L−1 for MA and 148.0 ± 4.7 mg L−1 for FGA) and stability tests. The values are unweighted arithmetical averages of accepted results and their uncertainties
are combined uncertainties enlarged by coefficient k=1, evaluated from the standard uncertainties of the interlaboratory comparison, homogeneity and stability tests.
Received: 17 September 2002 Accepted: 1 November 2002
Acknowledgement This work was supported by the Internal Grant Agency of Ministry of Health of the Czech Republic (Grant NJ/6784–3).
Presented at CERMM-3, Central European Reference Materials and Measurements Conference: The function of reference materials
in the measurement process, May 30–June 1, 2002, Rogaška Slatina, Slovenia
Correspondence to I. Šperlingová 相似文献
16.
17.
Adriaan M. H. van der Veen Thomas P. J. Linsinger Andree Lamberty Jean Pauwels 《Accreditation and quality assurance》2001,6(6):257-263
To serve as a measurement standard, a (certified) reference material must be stable. For this purpose, the material should
undergo stability testing after it has been prepared. This paper looks at the statistical aspects of stability testing. Essentially,
these studies can be described with analysis of variance statistics, including variant regression analysis. The latter is
used in practice for both trend analysis and for the development of expressions for extrapolations. Extrapolation of stability
data is briefly touched upon, as far as the combined standard uncertainty of the reference material is concerned. There are
different options to validate the extrapolations made from initial stability studies, and some of them might influence the
uncertainty of the reference material and/or the shelf-life. The latter is the more commonly observed consequence of what
is called ’stability monitoring’.
Received: 6 October 2000 Accepted: 4 December 2000 相似文献
18.
Marina Patriarca Ferdinando Chiodo Marco Castelli Federica Corsetti Antonio Menditto 《Microchemical Journal》2005,79(1-2):337
The Me.Tos. Project, started in 1983 and still running, is an external quality assessment (EQA) scheme for laboratories performing specialized analyses in occupational and environmental laboratory medicine. Besides the organization of EQA exercises, initiatives for further education of the participants and the harmonization of EQA procedures at a European level are carried out. Participation in EQA schemes allows laboratories to comply with the international standards for the quality and competence of testing and clinical laboratories. The organization of the scheme includes the preparation of control materials, their distribution to the participants, according to strategies aimed to avoid identification of the samples, the statistical analysis of the results and the evaluation of laboratories' performance according to international guidelines and criteria set by the organizers. An overview of the scheme operation and the current performances of participants will be given. 相似文献
19.
N. Majcen 《Accreditation and quality assurance》2003,8(3-4):108-112
The fact that various definitions and terminology applied to measurements in analytical chemistry are not always consistent
and straightforward, by not only answering the question ”what”, but also ”how”, leads to their various interpretations. This
results in non-uniform implementation of very basic and essential metrological principles in chemistry. Such a diverse situation
is not conducive to the endorsement of harmonised measurements all across the world, to serve as a tool for improving the
quality of life in its broadest sense for all its citizens. The discussion in this paper is focused on problems associated
with terminology and definitions of ’reference material’ and ’validation’. The role of reference materials in measurement
processes for purposes other than calibration and validation principles in analytical chemistry are also discussed in this
paper. Where possible, potential solutions are proposed, but more often, questions of essential importance are raised in order
to initiate international discussion which will hopefully lead to equally understandable answers.
Received: 2 November 2002 Accepted: 3 February 2003
Acknowledgements
The author is grateful to Aleš Fajgelj for his comprehensive comments on the topic described in this paper. Sincere thanks
also to Philip Taylor, Ewa Bulska, Emilia Vassileva, Miloslav Suchanek and Margreet Lauwaars for their contribution during
fruitful discussions on validation.
Presented at the CERMM-3, Central European Reference Materials and Measurements Conference: The function of reference materials
in the measurement process, May 30–June 1, 2002, Rogaška Slatina, Slovenia
Correspondence to N. Majcen 相似文献
20.
Adriaan M. H. van der Veen Thomas P. J. Linsinger Heinz Schimmel Andree Lamberty Jean Pauwels 《Accreditation and quality assurance》2001,6(7):290-294
The main objective of the certification of a reference material is to determine its property values including their uncertainty.
In the previous parts of this series, the basis for the evaluation of measurement uncertainty of the property values has been
examined, including the conversion of homogeneity and stability study data into standard uncertainties. In this final part,
the determination of the property values and the modelling of the certification process is discussed. It is noted that the
characterisation of a reference material can be modelled in some cases using analysis of variance statistics, but a more generally
applicable model can be developed based on χ2-fitting. Furthermore, it is concluded that there is an advantage in using absolute standard uncertainties instead of relative
ones when modelling the certification process.
Received: 14 October 2000 Accepted: 21 January 2001 相似文献