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It is important to protect critical buildings (shopping centres, government buildings and embassies), infrastructure and utilities, train and underground stations against being damaged, destroyed or disrupted by deliberate acts of terrorism, criminal activity and malicious behaviour. Normal regulations and building guidelines do not generally take into account these threats. The introduction of appropriate regulations or guidelines, where deemed necessary, should enhance the resilience of buildings and infrastructure against explosion incidents. In order to protect the built infrastructure, methods are required to quantify the resistance of structural components against explosive loading and to assess the hazards resulting from the failure of an element. The applicable state-of-the-art techniques may include either experimental or numerical methods, or a combination of both. Therefore, the thematic group (TG) on the resistance of structures to explosion effects was formed in order to bring the required expertise together, make it commonly available and to find and define harmonised methods and solutions which can be provided to the decision-makers responsible for critical infrastructure protection. This report discusses the differences between the existing standards for testing blast-resistant glazing and windows and it presents basic recommendations for the future development of the suite of European standards in this area.
A novel approach for rating fatigue-initiating inclusions in highly demanding steel (INCAFAT)
(2018)
INCAFAT project aimed to improve existing fatigue damage models by establishing the most suitable combination of measurement techniques to characterise harmful inclusion populations in highly demanding steels. The different inclusion assessments carried out confirm that, chemical composition, secondary metallurgy and manufacturing route affect content, nature, size and shape of inclusions. According to the FEM model, inclusions produce an alteration of the stress field in their surrounding region, which can promote a fatigue failure. Experimental work on fatigue testing has demonstrated that depending on the stressed direction fatigue failures in highly demanding steels could be produced by different types of inclusions. Fractography analyses confirmed that meso-inclusions harmful in fatigue cannot be rated by standard methods, nor 10 MHz ultrasonic testing (macro) or micro-cleanness assessments. The necessity of rating these meso-inclusions has led to critical evaluation of Extreme Value Analysis according to ASTM E2283-08 and the development of high frequency immersion ultrasonic testing. EVA methodology based on inclusion width can be applied reliably when principal stress is parallel to the rolling direction. On the contrary, if inclusions are testing in the elongated directions its fails. On the other hand, the guidelines and recommendations for high frequency ultrasonic testing have been compiled in a new European standard draft. This method based on focal beam probes and high-resolution devices is able to provide information on meso-inclusion distribution.
The determination of the blast protection level of laminated glass windows and facades is of crucial importance, and it is normally done by using experimental investigations. In recent years numerical methods have become much more powerful also with respect to this kind of application. This report attempts to give a first idea of a possible standardisation concerning such numerical simulations. Attention is drawn to the representation of the blast loading and of the behaviour of the material of the mentioned products, to the geometrical meshing, as well as to the modelling of the connections of the glass components to the main structure. The need to validate the numerical models against reliable experimental data, some of which are indicated, is underlined.
Typology of Inks
Archives and museums around the world contain a vast number of manuscripts that were written in different inks: carbon inks, plant inks, iron-gall inks and mixed inks. Yet most archaeometric studies of manuscripts focus on the palette of pigments found in illuminated manuscripts whereas identification of the inks is still largely based on cultural-historical studies and visual inspections. One of the reasons of this disproportion in the studies can be explained by the properties of Raman spectroscopy, the technique of choice for identification of pigments. In contrast, this technique is only partially viable when dealing with organic colourants. Brown and Clark discuss these difficulties and the uncertainties of identification of iron-gall inks by Raman spectroscopy in their pioneering work on early medieval Anglo-Saxon manuscripts (K. Brown and R. Clark 2004). To facilitate instrumental analysis of inks, we have developed a protocol that starts with the identification of the inks type (Rabin et al. 2012) which doesn’t require complicated instrumentation and can be carried out by paleographers and codicologists.
Three typological ink classes
The black writing materials used in manuscript production in Antiquity und Middle Ages can be sorted in three typologically different ink classes: soot, plant and iron-gall. Soot ink is a fine dispersion of carbon pigments in a water soluble binding agent; plant-based ink consists of a solution of the tannins extracted from gallnuts or tree bark; iron-gall ink, is produced by mixing a soluble compound of iron (II) with gallic or tannic acid extracted from gallnuts or tree bark. Therefore, iron-gall ink presents a boundary case between solution and dispersion ink, in which a water-soluble preliminary stage oxidizes and evolves into a black, insoluble precipitate similar to the carbon pigments when the writing is exposed to air (Krekel 1999). The additional category of mixed inks, i.e. inks produced by addition of various metals to the soot inks or intentional mixing of iron-gall and soot - based inks started attracting scholarly attention only recently because their significance was established only a short while ago (Brun et al. 2016, Colini 2018, Nehring et al. 2021). We suggest that plant and mixed inks build a bridge from the carbon ink of Antiquity to the properly formulated iron-gall ink that became a standard black ink from the late Middle Ages to the 19th century when it gave way to modern inks.
The committees ISO/IEC JTC1/SC28 and DIN-NI-28 "Information technology, Office equipment" have
worked together to develop the International Standard ISO/IEC 15775. The new national standards
DIN 33866-1 to 5 (in print, drafts May to Nov. 1999) and the International Standard ISO/IEC 15775
are based on equivalent colour series. Both use the same colour series both in digital and analog test
charts and approximately the same layout.
New colorimetric technologies of Germany and Japan have been used to produce the four DIN- and
ISO/IEC-test charts in offset printing (3600 dpi) which are in application for colour devices now.
The different productions will be shown, e. g. in halftone and continuous tone and in reflectance and
transmittance mode. Some problems of measurement (e. g. fluorencent photographic material) and the
accuracy of production is important for applications.
A flat area lamp which is shown at the conference has the chromaticity of D65. With transparent ISO/IEC-test chart material on top this equipment defines a reference monitor for comparison with display
output. For additional information see the URL: www.ps.bam.de
Four ISO/IEC-test charts in different modes (halftone
and continuous tone, in reflectance and
transmittance mode) have been defined in ISO/IEC
15775 and ISO/IEC DIS 19839-1 to 4 to
specify image reproduction properties of colour
copiers, printers, scanners and monitors.
Corresponding test charts have been defined in DIN
33866-1 to 5.
All colours of all test charts are defined in CIELAB
coordinates. Main colour series are equally spaced
in CIELAB colour space both in lightness L* and
chroma C*. Up to now there are productions of DIN
and JBMA (Japan Business Machine Makers
Association) according to ISO/IEC 15775 which can
be used for all applications.
Assessment of existing steel structures - Recommendations for estimation of remaining fatigue life
(2008)
This report describes the progress in understanding and describing the detectability of the ultrasonic inspection technique developed by SKB for the inspection of copper tubes used for the final disposal of the Swedish spent nuclear fuel. In former research activities dedicated to the different parts of the canister, the probability of detection (POD) evaluation technique, as developed for thin aircraft components, was further developed for the application on complex hick-walled components. The result of this development was the introduction of a “multi-parameter” POD framework. In contrast to taking only the defect size into consideration (as for aircraft components) additional influencing factors, relevant for thick components, such as depth position, orientation and part geometry, were included. Furthermore, the variation of ultrasonic attenuation due to various material properties was included.
Four ISO/IEC-test charts have been defined in ISO/IEC 15775 (1999) to specify image reproduction of
colour copiers. Corresponding test charts have been defined in DIN 33866-1 to 5 (in print) to specify
image reproduction of colour copiers, printers, scanners and monitors. All colours of all test charts are
defined in CIELAB coordinates. In applications the devices including software are used for test chart
input and output in the three different combinations "analog - analog" (copiers), "digital - analog"
(printers, monitors) and "analog - digital" (scanners, Photo-CD-systems).
This paper uses mainly ISO/IEC-test colours of a 16 step grey scale (defined by olv*-coordinates
according to the standard) in the original scene to calibrate the variable (photographic and Photo-CD)
analog-digital process. The relative digital olv*-input data and the digital olv*'-output data are used to
get approximately the same digital output (image file) independent of exposure (e. g. between -1 stop
under to +2 stop over exposure for slide or negative film) and other variables, e. g. the digitizing Photo-
CD-process. This "direct" colour management method adds a new method compared to the ICC colour
management method which fails to handle variable processes and can not manage the variable data of
original scenes taken by the photographic process.
Building products: Determining and avoiding pollutants and odours - Results from a research project
(2007)
Isotope amount ratios (hereafter referred to as simply isotope ratios) are proving useful in an ever increasing array of applications that range from studies unravelling transport processes, to pinpointing the provenance of specific samples as well as trace element quantification by using isotope dilution mass spectrometry (IDMS). These expanding applications encompass fields as diverse as archaeology, food chemistry, forensic science, geochemistry, medicine and metrology. However, to be effective tools, the isotope ratio data must be reliable and traceable to enable the comparability of measurement.
The importance of traceability and comparability in isotope ratio analysis has already been recognized by the Inorganic Analysis Working Group (IAWG) within the CCQM. Three pilot studies have focused on the quality of isotope ratio determinations (P48 “U isotope ratios in urine”, P75 “stable isotopes in Methionine”, P105 “87Sr/86Sr in wine”). Moreover, isotope ratio measurements are fundamental to IDMS amount of substance determinations. For example, when Pb quantification using IDMS is undertaken, this requires the measurements of Pb isotope ratios. While the requirements for isotope ratio accuracy and precision in the case of of IDMS are generally quite modest, “absolute” Pb isotope ratio measurements for geochemical age dating and source rock characterization as well as forensic provenance and fingerprinting studies require Pb isotope ratio measurements of the highest quality. To support present and future CMCs on isotope ratio determinations, a Key Comparison was urgently needed. Therefore, it was decided at the IAWG meeting in Paris in April 2011 that a Key Comparison on the determination of Pb isotope ratios in a pure Pb solution and in a bronze sample should be organized and accompanied by a pilot study.
Measuring Pb isotope amount ratios in a pure Pb solution, while seemingly straight forward, rigorously tests the ability of analyst to correct for any instrumental effects (such as mass discrimination and blank correction) on the measured ratios. Pb, present in trace amounts in a metal matrix sample (e.g. Pb in bronze), provides a real world test of the whole chemical and instrumental procedure, from chemical separation and sample purification to analysis and subsequent correction of appropriate instrumental effects on the separated samples.
A suitable bronze material with a Pb mass fraction between 10 and 100 mg·kg-1 was available at BAM. A high purity solution of Pb with a mass fraction of approximately 100 mg·kg-1 was also available. By comparing the Pb isotope ratio results obtained for the bronze sample with the Pb isotope ratio results from the Pb solution, potential biases arising from the processing of the bronze sample could be effectively identified and separated from the instrumental effects arising from the measurement and data processing protocol.
The cement proficiency testing (PT) scheme was set up by the German Metrology Institute (PTB) and the Federal Institute for Materials Research and Testing (BAM) in 2012. The PT scheme was a spin-off from a European Commission and African, Caribbean and Pacific-Group of States funded project entitled SPIN – Spearhead Network for Innovative, Clean and Safe Cement and Concrete Technologies (www.spin.bam.de). The SPIN project aimed at crosslinking experts in industry and policy making bodies, with the prospect of establishing a sustainable cement and concrete construction capacity in Africa.
After a successful first pan-African proficiency testing scheme in 2012/2013, it was decided to establish the scheme permanently and independent of the SPIN project.
The main focus of setting up a testing scheme was to enable all cement testing laboratories in Africa to evaluate their competence and efficiency in cement testing and further enhance their capacity to obtain better quality products according to their environment. The acronym developed for the PT scheme is PACE-PTS (Pan-African Cement Proficiency Testing Scheme). The framework for the PT scheme was set up jointly among the organisers and the first participants. The first PT scheme was initiated in Dar Es Salaam in 2012 followed by a final workshop in Berlin in 2013. The second PT scheme began in 2014. A final workshop was organised in Dar es Salaam in 2015. The third and current scheme was started in 2016 and the final workshop is held in Yaoundé.
This Report describes the certification of the reference material antimony implanted in Si/SiO2 intended to be used for calibration of surface and near surface analytical methods. It describes the preparation, homogeneity measurements and the analytical work performed for the certification of both Areal density of antimony Atoms (retained dose) and the isotope amount Ratio as well as giving considerations on the stability of the material.
Three petrol reference materials were certified for their total sulfur content in support of Directive 2003/17/EC of the European Parliament and of the European Council, which stipulates that petrol with a maximum S content of 10 mg/kg must be available in all member states by 2009. Commercially available petrol was obtained and filled into borosilicate ampoules without further treatment. Homogeneity of the materials was tested and no heterogeneity was detected for two of the materials, whereas minor heterogeneity was observed for the third material. Stability of the materials was tested for 8-12 months at 60 °C and no degradation was observed. Characterisation was based on isotope-dilution mass spectrometry (IDMS) applied as primary method of measurement by three European metrology institutes and certified values were assigned using all results. The certified uncertainties include contributions of (potential) heterogeneity, potential degradation as well as characterisation. The final assigned values are:
ERM-EF211: 48.8 ± 1.7 mg/kg
ERM-EF212: 20.2 ± 1.1 mg/kg
ERM-EF213: 9.1 ± 0.8 mg/kg
The materials are available from IRMM (ERM-EF211), LGC (ERM-EF212) and BAM (ERMEF213)
Lead (Pb) isotope amount ratios are commonly used in applications ranging from archaeology and forensic sciences to terrestrial and extra-terrestrial geochemistry. Despite their utility and frequency of use, only three certified isotope amount ratio reference materials are currently available for Pb: NIST SRMs 981, 982 and 983. Because SRM 981 has a natural Pb isotopic composition, it is mainly used for correcting instrumental mass discrimination or fractionation. This means that, at present, there are no other certified isotope reference materials with natural Pb isotopic composition that could be used for validating or verifying an analytical procedure involving the measurement of Pb isotope amount ratios.
To fill this gap, two new reference materials, both certified for their Pb isotopic composition, have been produced together with a complete uncertainty assessment. These new reference materials offer SI traceability and an independent means of validating or verifying analytical procedures used to produce Pb isotope amount ratio measurements.
ERM-EB400 is a bronze material containing a nominal Pb mass fraction of 45 mg/kg. ERM-AE142 is a high purity solution of Pb with a nominal mass fraction of 100 mg/kg. Both materials have been specifically produced to assist analysts in verifying or validating their analytical procedures. Note that while one of these reference materials requires the chemical separation of Pb from its matrix (ERM-EB400), the other does not (ERM-AE142). Details on the certification of these isotope reference materials are provided in this report.
Certification report for the reference materials ERM-AE102a, -AE104a, -AE120, -AE121 and -AE122
(2010)
Isotope reference materials are essential to enable reliable and comparable isotope data. Besides the correction of mass fractionation or mass discrimination isotope reference materials are indispensible for validation and quality control of analytical procedures. This article describes the production and certification of a set of five isotope reference materials ERM-AE102a, 104a, AE120, 121 and 122, for boron isotope analysis. The isotopic composition of all materials has been adjusted by mixing boron mother solutions enriched in 10B or 11B with a boron mother solution having natural-like isotopic composition under full gravimetric control. All mother solutions have been analysed for their boron mass fraction as well as their boron isotopic composition by TIMS using IDMS as calibration technique. For all five reference materials the isotopic composition obtained on the basis of the gravimetric data agrees very well with the isotopic composition obtained from different TIMS techniques. Performed stability and homogeneity studies show no significant influence on the isotopic composition as well as on the related uncertainties.
The certified isotope abundances for 10B are 0.29995 (27) for ERM-AE102a and 0.31488 (28) for ERM-AE104a. The certified δ11B values are -20.2 (6) ‰ for ERM-AE120, 19.9(6) ‰ for ERM-AE121 and 39.7 (6) ‰ for ERM-AE122.
Together with the formerly certified ERM-AE101 and -AE103 a unique set of seven certified reference materials (CRM) for boron isotope analysis is now available from BAM.
Isotope reference materials are essential to enable reliable and comparable isotope data. Besides the correction of mass fractionation or mass discrimination, isotope reference materials are indispensible for validation and quality control of analytical procedures. This report describes the production and certification of two isotope reference materials, ERM-AE123 and ERM-AE124, for boron isotope analysis. The isotopic composition of ERM-AE123 is the unaltered natural-like isotopic composition of the base material. The isotopic composition of ERM-AE124 has been adjusted by mixing two boron stock solutions enriched in 10B and 11B respectively under full gravimetric control. All stock solutions have been prepared fully under gravimetrical control. The corresponding boron isotopic composition has been analysed by TIMS. For both reference materials the isotopic composition obtained on the basis of the gravimetric data agrees very well with the isotopic composition obtained by TIMS. The certified isotope abundances for 10B are 0.19832 (21) for ERM-AE123 and 0.96006 (6) for ERM-AE124. Together with the formerly certified ERM-AE101, -AE102a, -AE103, -AE104a, -AE120, -AE121 and AE122, a unique set of nine certified reference materials (CRM) for boron isotope analysis is now available from BAM covering a range for the 10B isotope amount fraction from 0.2 to 0.96 and for the δ11B value from -20 ‰ to +40 ‰.
Isotope dilution mass spectrometry often is applied for the quantification of platinum group elements in environmental and geological samples. In most cases, however, certified spike solutions offering complete uncertainty statements and SI-traceability are missing. This report describes the production and certification of two isotope reference materials, ERM-AE140 and ERM-AE141, serving as calibrated spike solutions for IDMS based quantification of Pd and Pt, respectively. Both materials were produced by dissolving highly enriched isotopes 106Pd and 194Pt and determining the mass fraction of 106Pd and 194Pt in the final solution by reverse IDMS. Two independent back-spikes were produced for each material from high purity Pd and Pt. Characterization measurements were carried out by MC-ICPMS. For ERM-AE140 the certified mass fractions are w(106Pd) = 20.24(5) mg/kg and w(Pd) = 20.54(5) mg/kg. For ERM-AE141 the certified mass fractions are w(194Pt) = 18.18(11) mg/kg and w(Pt) = 19.90(12) mg/kg. These values are traceable to the International System of Units (SI) in the shortest possible way.
The international research project HYCREF, funded by the European Commission in the 5 th Framework programme, aimed to develop methods to prepare homogenous and stable water-, soiland waste reference materials contaminated with mineral oil hydrocarbons and to test certify the mineral oil content by gas chromatographic methods. As mineral oil products are important sources for environmental contaminations a high need exists for certified reference materials for their determination using the new gas chromatographic methods (soil: ISO/FDIS 16703, waste: ENpr 14039, water: ISO 9377-2). The experimental conditions and results for preparation and characterisation of a total of nine reference materials (3 water-, 3 soil- and 3 waste materials) are described and discussed. Target values for the reference materials were defined at the beginning of the project in order to have clear quality criteria, which could be compared with the achieved results at the end of the project. These target specifications were related to the maximum uncertainty from test certification exercises (< 5 % for soil/waste and < 10 % for water), the maximum inhomogeneity between bottles (< 3 %) and minimum requirements for stability (> 5 years for soil/waste and > 2 years for water). The feasibility studies showed that solid materials (soil, waste) could be prepared sufficiently homogenous and stable. The test certified values of the 6 solid materials comprise a wide range of mineral oil content from about 200-9000 mg/kg with expanded uncertainties between 5.7-13.1 % using a coverage factor k (k = 2). The development of new water reference materials –the so-called “spiking pills” for an offshore- and a land-based discharge water represents one of the most innovative aspects of the project. The spiking pill technology facilitates the application and storage and improves the material stability compared with aqueous materials. Additional to the preparation and test certification of the reference materials investigations on the analytical method for the determination of mineral oil hydrocarbons were performed. The results obtained in relation to the optimisation of analytical method (extraction procedure, sample pretreatment, clean-up and measurement) were provided to the respective working group of ISO/TC 190, ISO/TC 147 and CEN/TC 292 and were incorporated into the ongoing standardisation procedures. The new version of ISO/FDIS 16703 (July 2004) includes the improvements based on HYCREF results, for example the increase of the solvent/sample ratio, the removal of acetone from the organic extracts and the use of column technique instead of batch technique for clean-up.
This report is a literature review of the current state of knowledge of fireworks
and fireworks hazards. It presents work to meet Deliverables D4-1 (types and compositions
of fireworks Articles), D4-2 (Functioning mechanism of and between fireworks
articles), D4-3 (Storage and transport regulations in EU countries) and D4-4 (The effect
of fireworks on health and the environment) of the CHAF work program.
Firework compositions are discussed in the first section. This leads to an understanding
of the variability in performance of various types of fireworks. Compositions
used in report effects are highlighted as being the most energetic while other compositions
are seen as providing a much lesser hazard in mass storage of fireworks. Individual
types of firework are examined. Large devices such as report shells are identified as
posing the largest hazard in bulk storage. Lesser, but still significant, hazards are predicted
for similar compositions in Roman candles and rockets. Gradations in hazard are
identified corresponding to UN hazard divisions 1.1, 1.3 and 1.4.
The second section reports the literature relating to the functioning mechanism of
and between fireworks articles. In this the major propagation mechanisms for fireworks
compositions are examined. The main stimuli identified are: fragment impact, heat and
shock wave, each of which can lead to the functioning of pyrotechnic composition in
the article or in an adjacent article leading to large-scale initiation. Consideration of the
pyrotechnic compositions leads to a different ranking for the three mechanisms with different
fireworks types. Thus with a report composition containing a metal/perchlorate
mixture shock initiation is seen to be the main propagation mechanism. Such a mechanism
is likely to afford a mass explosion. At a lesser hazard, blackpowder-based compositions
are reported to be more likely to propagate via a flame mechanism. This is less
likely to produce a mass explosion.
National legislation concerning the storage of fireworks for many European countries
is considered in the third section. Many of the national regulations are based on a
cube root of explosives content to determine "safety distances", often written as Q1/3.
Different multiplying factors are then applied depending on the type of adjacent site
(production buildings, residential housing, roads etc.). Commonly 22Q1/3 is used for residential
dwellings. Special provisions are enacted in many countries either to allow
lesser distances or in some cases to increase the safety distances depending on the
perceived hazard or extenuating circumstances.
The final section deals with the environmental hazards posed by the use of
fireworks. Toxic effects of the materials used in the manufacture and the likely reaction
products from functioning fireworks are highlighted. These range from heavy metal
poisoning from metals present for their colour effect to respiratory problems due to
pyrotechnic fume (both particulate and gaseous). Finally, noise pollution is considered.
While there is a short term problem from pyrotechnic fume at times of high usage
(national celebrations) there is no literature evidence, as yet, of long term detriment to
the environment.
This is the first part (Deliverable 6-1) of workpackage 6 (WP6) in the framework of a research project funded by the European Community on the "Quantification and control of the hazards associated with the transport and bulk storage of fireworks" which was given the acronym CHAF. The work in this package aims to characterize selected packaged fireworks in standard UN classification tests by measuring the physical conditions (temperature, pressure, radiation, etc.), acting during testing and to use the results to provide benchmark data for the rest of the CHAF project. The objective of Deliverable 6-1 was to identify the types of fireworks that should be used for the benchmarking tests. This was achieved by developing the information generated in the literature review for the project (WP4). A critical element of the work was to attempt to identify fireworks close to the boundaries between different UN Hazard Divisions so that the accuracy of the UN classification assignments, as applied to fireworks, could be tested. This document outlines the types of fireworks selected for benchmark testing and the rationale behind the selection. Having identified the fireworks required a way forward to identify suitable suppliers is given.
Anwendungen von Bioziden in Materialien für Außenanwendungen sind mögliche Quellen für Biozide in Umweltkompartimenten infolge von witterungsbedingten Auswaschprozessen. Im Bericht werden Leachingprozesse und -parameter als auch Methoden zu deren Untersuchung unter Labor- und Freilandversuchsbedingungen beschrieben. Vorteile und Grenzen der verschiedenen Herangehensweisen zur Untersuchung von Leachingprozessen werden diskutiert. Standardisierte Auswaschtests sowie in der Fachliteratur publizierte Auswaschexperimente werden zusammenfassend dargestellt. Es wird beschrieben, wie Leachingdaten gemäß Technischem Leitfaden zur Biozidprodukten-Richtlinie 98/8/EG für eine Risikobewertung genutzt werden. Ein alternativer Ansatz zur mathematischen Modellierung von Leachingtest-Daten wurde erprobt und wird im Bericht erläutert. Potentiell lassen sich mit dem vorgeschlagenen Ansatz bestimmte gegenwärtig auftretende Schwierigkeiten bei der Risikobewertung umgehen.
Applications of biocides in outdoor materials are potential sources of biocides in environmental compartments due to leaching processes under weathering conditions. Leaching processes and parameters as well as methods to investigate leaching processes under laboratory and semi-field conditons are described in the report. Benefits and limitations of different test approaches are discussed. Standardised leaching tests as well as leaching experiments reported in scientific literature are listed. The application of leaching data for risk assessments according to the Technical Guidance Documents for the Biocidal Products Directive (98/8/EC) is described. An alternative approach for mathematical modelling of leaching data was tested and is Explained in the report. Certain difficulties that currently appear during risk assessments may be circumvented by the proposed approach.
Novel martensitic filler materials with specially adjusted martensite start temperatures (Ms) can counteract the cooling specific shrinkage due to expansion effects of the weld metal associated with phase transformations. That can be exploited to create compressive residual stresses in the weld and adjacent areas, i.e. beneficial for increasing fatigue strength. The Ms temperature is shifted via the chemical composition, mainly by the alloying elements nickel and chromium, resulting as well in different retained austenite contents. Investigations were made using different Low Transformation Temperature (LTT) alloys with varying nickel content. The resulting phase transformation temperatures were - for the first time - detected using high energy synchrotron diffraction and Single Sensor Differential Thermal Analysis (SS-DTA). Compared to angle dispersive diffraction, energy dispersive diffraction offers the possibility to measure residual stresses of the martensite and austenite phase parallel fast in one experiment up to depths of 100 µm. The residual stresses show significant distributions dependent on Ms temperature. The effect on the cold cracking behaviour of these alloys was investigated using the Tekken test. Results show that cold cracking can be avoided when appropriate contents of retained austenite are existent.
A reflective and transparent ISO/IEC-test charts no. 3 according to ISO/IEC 15775 and DIS ISO/IEC 19839-1
to -4 is used for different tests of colour reproduction on printers and monitors in the office which is illuminated by
daylight D65. The reflective ISO/IEC-test chart produced by DIN and JBMA in offset printing has a contrast range of
1:35. The calculation and production of a transparent ISO/IEC-test chart is described which produces the same
contrast range for a standard 2.5% reflection condition. The transparent ISO/IEC-test chart has a contrast range of
1:10.000 and on top of the "white" monitor screen with the standard illumination of 500 lux the office lighting reduces
to the standard contrast range between black and white to 1:35. The office illumination changes additionally the 16
step spacing and the appearance of the 16 grey samples on the monitor of both the tranparent test chart on top and
of a digital test chart output. The contrast range and the spacing of the 16 grey steps for the printer and the monitor
output and the transparent ISO/IEC-test chart which is fixed on a "white" monitor screen can be made equal. The
reflective or transparent ISO/IEC-test chart allow to test many properties of the working place in the office, e. i. by
recognition of Landolt-rings, line screens, Siemens stars, 16-step spacing etc. The recognition and spacing is
highly influenced by the office illumination, the luminance and surface reflection properties of the monitor and the
imaging software.
The procedure to produce equidistant 16 step grey spacing for the printer and monitor output is described. The
digital ISO/IEC-test chart no. 3 which includes CIELAB L* lightness input data is used to produce a linear input -
output relationship. It is only necessary to replace the 16 linear (ideal) L* data in the ISO/IEC-test chart file (in
PostScript file format at the beginning) by the 16 L* output data of the printer or monitor output to produce the
intended equally spaced 16 step grey output. In the standard test chart file the L* lightness input data vary within the
standard range between L*=18.0 and L*=95.4. In the digital NP-file the L* data are used by the PostScript (PS)
operator L* setcolor for the standard CIELAB colour space. In the digital CP-file the L* data are transferred to
relative lightness w* which is zero for black N and 1 for white W and the PS operator w* setgray is used. The digital
FP-file includes a PostScript MTL code (Measurement, Transfer and Linearisation) which produces a linear
relationship between the w* input data (between 0 and 1) and the L* lightness output on any printer or monitor. It is
described how to use the reflective or transparent ISO/IEC-test charts to produce this linear relationship by visual
comparison (or CIELAB or XYZ measurement) with the reference. If the transparent BAM-test chart as refererence
is NOT available a training method with a digital test chart as reference is described which leads to the linear input -
output relationship. At present often monitors (and printers) show for the 16 grey steps of the achromatic ISO/IECtest
chart no. 3 mean differences of 10 in lightness L* (between 0 and 25). The method of this paper often allows to
reduce the lightness differences from 10 to less then 3 (by a factor 3 to 5). This is then below the tolerance of 3 which
is intended in ISO/IEC 15775 for colour copiers. So the output on different printers and monitors will be made very
similar.
Cleaning - A balancing act
(2006)
This text originally appeared as chapter 5, 'Reinigung - Eine Gratwanderung' (pp. 101-28) in A. Wolff (ed.), Restaurierung und Konservierung historischer Glasmalereien, Mainz, 2000.
Within the context of this research programme, scientists and conservators collaborated to assess various cleaning methods for historical stained glass. For cleaning glass surfaces there are the mechanical methods already being applied in most workshops, as well as the new chemical cleaning possibilities. Laboratory experiments were conducted initially on model glass in order to test the effectiveness and damage potential of these various methods; the model glass was examined both before and after cleaning by means of light microscopy and infra-red spectroscopy. In addition to this, cleaning tests were carried out on samples of original glass; electron-ray micro-analysis was also used to evaluate the results of these tests. The model-glass samples were corroded in advance by accelerated weathering in an attempt to simulate the damage seen on medieval glass. Enough model glass was prepared to allow any number of series of experiments to be carried out, in order to compare the effectiveness and suitability of the various chemical and mechanical methods and techniques.
For the mechanical cleaning tests, a wide range of selected tools was tested by different conservators on pre-corroded model glass. This showed clearly that the success (or lack of it) of a cleaning episode was determined not just the choice of tool, but by the skill with which conservator wielded it. This observation was later confirmed by research on samples of original glass. Insensitive handling of tools or unsuitable tools could damage or completely destroy the gel layer. The gel layer should not be damaged, as this leads to increased levels of corrosion subsequently, though the encrustations should be reduced, as their hygroscopic qualities accelerate the corrosion processes.
At the next stage, chemical cleaning methods were tested, and the results of cleaning with organic solvents (toluene, ethanol, acetone, etc.) and water-based solutions (oxalic acids, EDTA, ammoniac, etc.) compared with one another and evaluated. It became clear that strongly acidic and alkaline solutions, depending on the condition of the surface, could cause damage or have uncontrollable consequences.
In the specific case of the glass from Erfurt Cathedral, for whose firmly fixed, very hard, opaque encrustations mechanical methods proved to be either ineffective or damaging to the glass, new chemical cleaning possibilities had to be found. Following comprehensive preliminary tests on model glass, various types of ion-exchanger and ammonium-carbonate solution were chosen. Both methods were successful in improving the transparency of some (but not all) of the samples.
The experiments with the original material from Erfurt Cathedral clearly showed that successful cleaning was dependent on the particular composition of the encrustation. Really gentle cleaning can be achieved by chemical means, though only when the chemical agents are tailored to individual damage situations; this can only be achieved when scientific analysis is undertaken in tandem with the cleaning processes.
The assessment of these mechanical and chemical cleaning methods was oriented towards treating corrosion on sensitive medieval glass. Nineteenth-century glass is generally less sensitive, though cleaning of this material must also be careful and very gentle. Scientific analysis alone is not enough to determine the choice of cleaning method, but can act as an aid to the conservator in selecting the right cleaning agent and method.
This report gives technological information about processes for the recovery of phosphorus from sewage sludge ash including mass- and energy balance, process conditions and product quality.
The information in this report aim at giving an overview on different concepts for the recovery of phosphorus from sewage sludge ash and are intended to allow a general qualitative comparison between the different technical approaches. This report also describes the technological backgrounds of the processes that were furthermore investigated by life cycle assessment (LCA) and life cycle cost (LCC) analysis. However, most process data stated in this report are site specific data. The LCA/LCC study includes the definition of a common base line for all processes, detailed process modeling and plausibility assessments. Results of the LCA/LCC-studies are reported in deliverables D9.2 und D10.1.
This study was designed to examine and compare the operation of accreditation bodies in Europe. A management tool, the Process Maturity Benchmarking Tool (PMBT), was elaborated and validated by applying it to various accreditation bodies. By applying the tool, the values of indicators were determined, thus enabling a comparison of the accreditation bodies despite different operational processes and organizational forms.
The management tool PMBT is based on the analysis of selected processes with high relevance for the operation of accreditation bodies. The processes are derived from a process map designed for accreditation bodies in a universally applicable way. The indicators used to characterize the processes come from two sources: The first source relates to data already available from internal databases, reports, financial audits etc. The second source is derived from a self-evaluation of process maturity performed by the accreditation bodies. The criteria for evaluating process maturity were designed by applying the criteria of the EFQM excellence model 2013 of the European Foundation for Quality Management (EFQM) to the processes identified in the process map.
The project Comparison of the Operation of Accreditation Bodies in Europe comprised three stages. In the first stage, the processes of accreditation bodies were systematically analyzed. A process map was developed and processes of special relevance for the performance of accreditation bodies were identified and underpinned by indicators as described above. In the second stage, the processes of the German accreditation body DAkkS were assigned to the tool. This stage was used to check and modify the indicators when necessary. In the third stage, the transferability of the model was analyzed by extension to seven other accreditation bodies operating in Europe. The third stage of the project ended with a workshop attended by the eight accreditation bodies, which was used to present and discuss the results of the comparison and to identify best practices.
In 2019 the Bundesanstalt für Materialforschung und –prüfung (BAM) conducted a benchmarking to compare the operations of European accreditation bodies and to identify best practices, with the aim of improving key processes in accreditation. Ten European accreditation bodies attended the comparison, four of which had already taken part in the pilot phase of the benchmarking project, which was conducted in 2017 by the German accreditation body Deutsche Akkreditierungsstelle GmbH (DAkkS) and BAM.
The study, designed to examine and compare the operation of accreditation bodies in Europe, used a management tool called Process Maturity Benchmarking Tool, which was especially elaborated and validated for this purpose in the pilot phase, in order to determine the values of indicators, thus enabling a comparison of the accreditation bodies despite different operational processes and organizational forms. The management tool is based on the analysis of selected processes with high relevance for the operation of accreditation bodies. The processes are derived from a process map designed for accreditation bodies in a universally applicable way. The indicators used to characterize the processes come from two sources: The first source relates to data already available from internal databases, reports, financial audits, and others. The second source is derived from the self-evaluation of process maturity performed by the accreditation bodies. The criteria for evaluating process maturities were designed by applying the criteria of the EFQM excellence model 2013 of the European Foundation for Quality Management (EFQM) to the processes identified in the process map.
The results of the analysis were presented to and discussed with representatives of the ten accreditation bodies at a Results-Workshop that took place at BAM on 21/22 January 2020.
This study was designed to examine and compare the operation of accreditation bodies in Europe. A management tool, the Process Maturity Benchmarking Tool (PMBT), was elaborated and validated by applying it to various accreditation bodies. By applying the tool, the values of indicators were determined, thus enabling a comparison of the accreditation bodies despite different operational processes and organizational forms.
The management tool PMBT is based on the analysis of selected processes with high relevance for the operation of accreditation bodies. The processes are derived from a process map designed for accreditation bodies in a universally applicable way. The indicators used to characterize the processes come from two sources: The first source relates to data already available from internal databases, reports, financial audits etc. The second source is derived from a self-evaluation of process maturity performed by the accreditation bodies. The criteria for evaluating process maturity were designed by applying the criteria of the EFQM excellence model 2013 of the European Foundation for Quality Management (EFQM) to the processes identified in the process map.
The project Comparison of the Operation of Accreditation Bodies in Europe comprised three stages. In the first stage, the processes of accreditation bodies were systematically analyzed. A process map was developed and processes of special relevance for the performance of accreditation bodies were identified and underpinned by indicators as described above. In the second stage, the processes of the German accreditation body DAkkS were assigned to the tool. This stage was used to check and modify the indicators when necessary. In the third stage, the transferability of the model was analyzed by extension to seven other accreditation bodies operating in Europe. The third stage of the project ended with a workshop attended by the eight accreditation bodies, which was used to present and discuss the results of the comparison and to identify best practices.
Tensile testing according to EN 10002-1 is one of the basic mechanical tests to characterise the mechanical properties of metallic materials. This testing procedure has been regularly under development for many decades in order to modify and amend it and to bring it up to an up to date standard. Today tensile testing for quality control in metals manufacturing industry is routinely performed automatically with computer controlled testing machines. Due to economical needs of industry proposals were made by a European Standard Committee to amend the standard EN 10002-1. A European research project with the acronym TENSTAND was started to validate the proposed modifications of the tensile testing standard. The work package 4 of the project was to validate the machine control characteristics. A comparison test program was started with ten partners, 4 test piece geometries and 3 test parameters for 6 materials, partly with upper and lower yield strength and partly with 0.2 % proof strength to compare experimental results according to the proposal to modify the standard EN 10002-1. Initially testing in the strain control mode was introduced as well as switching of the control mode to crosshead control 1 and switching of the testing speed at appropriate points during the test. The comparison test was evaluated statistically and scientifically. The following conclusions were derived from the comparison test and summarised as recommendations to the standard committees. The scatter of the material properties were not significantly reduced by introducing the amended testing procedure. Few of the reasons for the continuously observed scattercan be identified as follows: The material properties are observed to be widely dependent on the testing speed. As a consequence the range for the allowed testing speed must be reduced. The closed loop control was not optimised sufficiently in some tests, the use of complicated testing machine software led to misinterpretation of software commands, individual testing equipment and implementation of the tensile testing procedure led also to scatter of the material properties which lay in a range of few percent. This is blurred by the inhomogeneity of the material.
The content of the paper is the assessment of the performance of (conventional) measurement techniques (MTs)with respect to the classification of disperse materials according to the EC recommendation for a definition of nanomaterial. This performance essentially refers to the accurate assessment of the number weighted median of (the constituent) particles. All data and conclusions are based on the analytical study conducted as real-world performance testing.
It comprised different types of MTs (imaging, counting, fractionating, spectroscopic and integral) as well as different types of materials. Beside reference materials with well-defined size distribution the study also included several commercial powders (variation of particle composition, morphology, coating, size range and polydispersity). In order to ensure comparability of measurement results, the participants were guided to use uniform protocols in sample preparation, conducting measurements, data analysis and in reporting results. Corresponding documents have been made public, in order to support the reviewing process of the paper, respectively to ensure the reproducibility of data by other users under the same conditions.
The scientific paper relies on a comprehensive set of revised measurement data reported in uniform templates, completely describes the experimental procedures and discusses the MTs’ performance for selected materials in detail. Even more, the study is summarised and evaluated, which leads to recommendations for the use of MTs within a tiered approach of NM characterisation. In addition, the paper critically examines the factors that may affect the outcome of such a comparison among different MTs.
The International Standard series ISO/IEC 15775
and DIS ISO/IEC 19839-1 to 4 for specifying
image reproduction properties of colour reproduction
processes analog-analog (copiers), analog-digital
(scanners) and digital-analog (printers, monitors)
seem to overlap with the International Standard
series IEC 61966-X for scanners, printers and
displays. But there are fundamental differences. In
the ISO/IEC standards the coding of colours is
based on reflective colours (defined for standard
offset printing) and in the IEC series on luminous
colours (defined for television).
Members of the standard groups ISO/IEC JTC1/
SC28 and IEC TC100 TA2 which developed the
above standards try at the moment to define
extended colour spaces (wide gamut colour spaces)
compatible with the present spaces of the standards
ISO/IEC 15775:1999-12 and IEC 61966-2-1:1999-
10.The extended spaces should match the
requirements of both the users and the industry for
the different applications. Important advantages and
disadvantages of both solutions based on coding of
reflective and luminous colours are presented.
In this research project, a new OECD Test Guideline (TG) for the determination of “Particle Size and Particle Size Distributions of Nanomaterials” was developed as the existing OECD TG 110 is considered to be outdated in terms of applicable size range (not covering sizes <200 nm) and methods. By its scope with an applicable size range from 1 to 1000 nm the new Test Guideline (TG PSD) covers the whole nanoscale. The TG PSD is applicable for particulate and fibrous nanomaterials. The prescribed, pairwise measurement of fibre diameter and length in the TG PSD allows for the first time to differen-tiate fibres with regard to their size-dependent hazard properties. Measurement instructions for each included method were validated within two separated interlaboratory comparisons, as a distinction between near spherical particles and fibres when applying the methods has to be made.
Besides information on content and structure of the TG PSD, this final report outlines essential steps, considerations and organisational aspects during the development of the TG. Insights into the selec-tion, preparation and prevalidation of test materials used in the interlaboratory comparison are given. Finally, main results of the interlaboratory comparisons and their impacts on the TG PSD are pre-sented.
Kurzfassung An neun verschiedenen Hardcopygeräten wurden in unterschiedlichen Emissionsmesskammern (zwei verschiedene 1 m³ - Kammern und eine 20 m³ - Kammer) in Kombination mit geeigneten Probenahme- und Analysenverfahren Untersuchungen zum Emissionsverhalten dieser Geräte hinsichtlich Staub, Ozon und VOC (TVOC) durchgeführt. Luftprobenahme und Analytik erfolgten für VOC mittels Tenax TA und anschließender Thermodesorption (TDS) in Verbindung mit GC / MS. Ozon wurde kontinuierlich bestimmt. Der Ozonanalysator arbeitete auf der Grundlage der flammenlosen Reaktion von Ozon mit Ethylen nach dem Prinzip der Chemilumineszenz. Die Staubbestimmung erfolgte gravimetrisch mittels Glasfaserfilter und Ultramikrowaage. Zusätzlich wurde die Partikelemission während des Druckbetriebes mit einem Partikelzähler bestimmt. Aufgrund der technischen Rahmenbedingungen standen nur kurze Druckzeiten von maximal 36 Minuten zur Verfügung. Um die Gleichgewichtskonzentration in der Prüfkammer zu erreichen, wurde die Luftaustauschrate in den 1 m³ - Kammern auf n = 4,0 bis 4,7 pro Stunde erhöht. Zusätzlich zur Prüfung in den Emissionsmesskammern sind verschiedene Papiere mittels Direkt - TDS sowie unter- schiedliche Toner mittels Headspaceprobenahme in Kombination mit GC / MS hinsichtlich ihres Emissionsverhaltens untersucht worden.
Für die untersuchten Geräte wurden Emissionsraten ermittelt. Sie betrugen für TVOC 0,41 bis 22,4 mg pro Stück und Stunde, für Ozon kleiner 0,02 bis 4,6 mg pro Stück und Stunde sowie für Staub 0,10 bis 7,63 mg pro Stück und Stunde. Verglichen mit Frischfaserpapier wurden bei den Untersuchungen mit Recyclingpapier deutlich höhere SVOC - Konzentrationen nachgewiesen. Im Ergebnis der Untersuchungen wurde ein Prüfverfahren entwickelt, das die Basis für Emissionsmessungen im Rahmen der Umweltzeichen RAL UZ 62, RAL UZ 85 sowie des neuen RAL UZ 114 für Multifunktionsgeräte darstellt. Abstract The emission behaviour with regard to dust, ozone and VOC (TVOC) of nine different hardcopy devices in combination with suitable air sampling and analysis procedures was investigated in different emission test chambers (two different 1 m³ - chambers and one 20 m³ - chamber). Air sampling and analysis for VOC were done by means of Tenax TA and subsequent thermal desorption (TDS) in connection with GC / MS. Ozone was determined continuously. The ozone analyser worked on the basis of the flame rid reaction of ozone with ethylene according to the principle of chemiluminescence. The dust determination was done gravimetrically by means of glass fibre filter and an ultra micro - balance. Additional the particle emission during the printing process was measured with a particle counter. The general technical conditions of the tested hardcopy devices were the reason for short printing times with a maximum of 36 minutes. In order to achieve the equilibrium concentration in the test chambers the air exchange rate in the 1 m³ - test chambers had to be increased to a value of n = 4,0 to 4,7 per hour. Additional to the examination of the hardcopy devices in the emission test chambers different papers were investi- gated by means of direct - TDS and different toners were tested by means of head space sampling in combination with GC / MS. For the examined hardcopy devices emission rates were determined. The emission rates for TVOC ranged from 0,41 to 22,4 mg per piece and hour, for ozone from less than 0,02 to 4,6 mg per piece and hour and for dust from 0,10 to 7,63 mg per piece and hour. The comparison between recycling paper and paper produced from primary fibres showed in general higher SVOC emissions from recycling paper. As the result of the investigations a test method for the determination of emissions from hardcopy devices was developed. This test method is the basis for emission tests in the framework of the German Award of the Environmental Label for office devices RAL -UZ 62, RAL -UZ 85 and the new RAL -UZ 114 for multifunctional devices.
The VSSA approach has the important advantage over classifying, imaging and counting techniques that it does not involve dispersion protocols. Further, the BET technique as the basis for VSSA determination it is in widespread use, generates low costs and is specified for many commercial materials. Finally, the same equipment allows for a deeper analysis by full isotherm evaluation.
The present deliverable assesses all NanoDefine powders, supplemented by further real-world materials (in total 26 powders), and quantitatively compares the relationship between the median size (by Electron Microscopy – considered as benchmark for the EC nanomaterial definition) vs. the size derived from VSSA. The VSSA method mitigates the challenges of EM to assess the thickness of platelets, but worked as well on fibbers and particles of irregular shapes. A screening strategy is proposed. If applied to the further data from real-world materials as validation set, this screening does achieve a correct classification, leaving only borderline materials for tier 2 assessment.
The four analog ISO/IEC-test charts in reflectance mode according to ISO/IEC 15775 are designed for
the test of colour copiers. The test charts include many image elements. e. g. Siemens-stars, Landoltrings
and 16 step equally spaced colour scales according to CIELAB. Most important for image
technology is the ISO/IEC pictorial image B1 which includes a 16 step grey scale and 16 CIE-test
colours.This image comes in 5 resolutions between 128 x 192, 256 x 384, and 2048 x 3096 pixels. For
analog production the digital ISO/IEC-test charts are described in ISO/IEC 15775.
Some applications of the digital and analog ISO/IEC-test charts for printers, monitors and scanners will
be discussed. Recently three methods to optimize the ISO/IEC-test chart output have been developed.
Between the digital input values and the CIELAB colour difference of the 16 step colour series a linear
relationship is produced. This linear property allows new and very simple colour management methods.
The application of these methods for the production of the reference ISO/IEC-test charts and for colour
management of slide and negative film images as function of exposure is shown.