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排序方式: 共有77条查询结果,搜索用时 31 毫秒
1.
Thomas P J Linsinger Alexander Bernreuther Philippe Corbisier Marta Dabrio Håkan Emteborg Andrea Held Andrée Lamberty Gaida Lapitajs Marina Ricci Gert Roebben Stefanie Trapmann Franz Ulberth Hendrik Emons 《Accreditation and quality assurance》2007,12(3-4):167-174
The potential approaches for third-party assessment of reference material producers are revisited and the activities of the
Reference Materials (RM) Unit of the Institute for Reference Materials and Measurements (IRMM) to obtain accreditation to
ISO Guide 34 and ISO 17025 are described. Accreditation was related to the Unit as all matrix RM activities of the institute
are concentrated there. A management system was established that allows sufficient flexibility to be applicable to a wide
range of RMs while being precise enough to ensure compliance with ISO Guides 30, 31 and especially 34 and 35. Accreditation
was achieved in 2004 with independent scopes for testing and RM production and was confirmed and extended in 2005. The key
aspects of the RM Unit's management system for RM production are presented.
Presented at BERM-10, April 2006, Charleston, SC, USA 相似文献
2.
An alternative method for stability testing of candidate certified reference materials (CRMs) utilizing “isochronous” measurements based on a storage design (storing samples at different temperatures for different time periods), which allows all measurements to be done at the same time, i.e. at the end of the study, is compared to “classical” designs of stability studies using reference time or reference temperature. The execution of stability studies using “isochronous” measurements only requires repeatability conditions, whereas classical designs require both repeatability and long term reproducibility conditions. Consequently, the new design allows the quality of results to be improved. 相似文献
3.
Linsinger TP Gawlik BM Trapmann S Lamberty A Emons H 《Analytical and bioanalytical chemistry》2004,378(5):1168-1174
Over the years, the nature of CRMs has changed considerably. Recently, more and more CRMs have been certified in their "natural" form, that is processed as little as possible, with analytes at their natural concentration level. This and the trend towards certified properties other than the concentrations of clearly defined molecules/elements have made guaranteeing stability of CRMs and estimating a shelf life an even more important issue for reference material producers than it has been before. One way to meet this challenge is to take more care in processing, storage and dispatch of CRMs. At IRMM, approximately 20 % of the RMs are stored at –20 °C or below and about 10% require cooled transportation. In addition, increased efforts for assessing stability are needed. Shelf lives are estimated using addition of an uncertainty component based on real-temperature stability studies rather than by accelerated stability studies. These pre-certification efforts are complemented by a stability-monitoring program, which at IRMM includes 80 % of the non-nuclear and non-isotopic materials. Although the costs for these efforts are high in absolute terms, they are only a minor and indispensable contribution to the total costs of CRM production. 相似文献
4.
5.
Zusammenfassung In dieser Arbeit wurden Schlußfolgerungen über den simultanen Verlauf der beiden Reduktionsphasen von Resazurin überprüft.Weiters wurden Bedingungen für die quantitative titanometrische Bestimmung von Resazurin und seiner Derivate ermittelt.
Mit 4 Abbildungen 相似文献
The conclusions about the simultaneous course of reduction of Resazurin to Resorufin and Resorufin to Dihidroresorufin were verified in this work.The conditions for the quantitative titanometric determination of Resazurin and its derivatives were found.
Mit 4 Abbildungen 相似文献
6.
Summary Lithium was determined in two BCR Candidate Reference Materials 303 and 304 by Isotope Dilution Mass Spectrometry using the state-of-the-art performance of isotope-specific methods gained during previous certifications of 6LiF reference targets used for the determination of the neutron lifetime [1]. After reconstitution of the serum, four aliquots of each of the two candidate materials from four different bottles were spiked with a previously characterized enriched 6Li spike [2] which is now available as CBNM IRM-615 and has a certified 6Li/7 Li ratio of 21.78±0.12 and a certified lithium concentration of 4.001±0.028 mol/g solution. The serum aliquots were digested in an HNO3/H2O2 mixture and after evaporation of the acid, the lithium was separated on a cation exchange column, eluted with 0.3 mol/L HCl and used as LiCl for mass spectrometric measurement on an NBS type thermal ionization mass spectrometer. Similarly an unknown sample BCR X, provided by BCR to check the performance of the certifying laboratories, was analyzed. In addition the chemical preparation method was controlled by assaying NBS (NIST) SRM 909. The chemical blank was determined by IDMS using 6Li enriched CBNM IRM-615. The measurements were corrected for isotopic fractionation using the Isotopic Reference Material CBNM IRM-016 chemically prepared in the same way as the samples. The CRM samples as well as the BCR X sample and the NBS SRM 909 were also analyzed for isotopic composition to verify whether they had indeed natural isotopic composition. The final results have an overall uncertainty of 1.2 and 1.5%, respectively. This overall uncertainty (on a 2s basis or an estimate thereof) takes into account all uncertainty contributions of statistical as well as of systematic nature (uncertainties on used reference materials, density and blank determinations). The final results compare favorably with the values proposed by BCR for certification, but have a smaller (better) uncertainty: CRM 303: (0.517 4±0.005 7) mmol/L, CRM 304: (0.987±0.014) mmol/L 相似文献
7.
T. P. J. Linsinger J. Pauwels H. Schimmel A. Lamberty A. M. H. van der Veen G. Schumann L. Siekmann 《Analytical and bioanalytical chemistry》2000,368(6):589-594
Uncertainties of four enzyme-CRMs that have recently been certified in a co-operation between the IRMM and the International
Federation for Clinical Chemistry were estimated. Estimation was based on the sum of the uncertainties of characterization,
homogeneity and stability. Data from the certification collaborative study were used to estimate laboratory uncertainties,
which form the basis for the uncertainty of characterization. Estimations for the uncertainty of homogeneity were derived
from classical homogeneity studies. The estimations of uncertainty of stability caused the most difficulties. Realistic uncertainties
fitting the needs of customers while being derived from measurement data based on theoretical considerations were obtained.
Received: 11 May 2000 / Revised: 21 June 2000 / Accepted: 27 June 2000 相似文献
8.
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
9.
10.
To play their role as essential tools for the achievement of comparability and traceability of measurements, the upcoming generation of certified reference materials will continue to be the subject of increased requirements related to their preparation, characterization, monitoring, documentation, and distribution. An analysis is made of the most important aspects not only related to the physical form of future CRMs, the determination of their shelf-life, and their certification, but also to increased requirements related to their distribution, including required additional documentation. Two examples of cost breakdown demonstrate the need for improved productivity of certification projects and more efficient marketing. 相似文献