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Laboratory test results are of vital importance for correctly classifying and labelling chemicals as “hazardous” as defined in the UN Globally Harmonized System (GHS) / EC CLP Regulation or as “dangerous goods” as defined in the UN Recommendations on the Transport of Dangerous Goods. Interlaboratory tests play a decisive role in assessing the reliability of laboratory test results. Interlaboratory tests performed over the last 10 years have examined different laboratory test methods. After analysing the results of these interlaboratory tests, the following conclusions can be drawn:
1. There is a need for improvement and validation for all laboratory test methods examined.
2. To avoid any discrepancy concerning the classification and labelling of chemicals, the use of validated laboratory test methods should be state of the art, with the results accompanied by the measurement uncertainty and (if applicable) the probability of incorrect classification.
This paper addresses the probability of correct/incorrect classification (for example, as dangerous goods) on the basis of the measurement deviation obtained from interlaboratory tests performed by the Centre for quality assurance for testing of dangerous goods and hazardous substances (CEQAT-DGHS) to validate laboratory test methods. This paper outlines typical results (e.g. so-called “Shark profiles” – the probability of incorrect classification as a function of the true value estimated from interlaboratory test data) as well as general conclusions and steps to be taken to guarantee that laboratory test results are fit for purpose and of high quality.
The biodeterioration of water-based manufactured formulations, such as polymer dispersions, is a major problem for the producing companies and the users of such products. Industrial preservatives, also known as biocides, are therefore used to protect these and similar products from the effects of microorganisms, predominantly bacteria and yeasts. In the absence of internationally recognised standard methods for determining the resistance of polymer dispersions to microbial growth and the efficacy of biocides used in them, protocols for testing other products, e.g., paints, have been adapted, and other methods produced by manufacturing companies, test laboratories, and academic institutions have been used. Often these do not take into account the specific nature of the materials being tested, the types of organism commonly causing contamination, and the conditions that the polymer dispersions will be exposed to during manufacture, storage, and use. By conducting a series of round-robin, collaborative tests, the member organisations of the International Biodeterioration Research Group Polymer Dispersion Working Group have identified the bacteria that commonly infect polymer dispersions, defined the main parameters necessary for a standard method of test, and developed a protocol that is robust, repeatable, and reproducible. The recommended test involves three repeat inoculations of the material with a previously determined mix of seven Gram-negative bacteria and evaluation of living cells by a simple plating technique. The work reported here, carried out by nine participating laboratories, is a final statistical validation and suggests that the method is eminently suitable as a standard test method.
Characterisation of the fibre/matrix interface in reinforced polymers by the push-in technique
(1997)
The push-in test is the only micromechanical test method that is not restricted to artificial fibre/matrix arrangements, but allows the in situ characterisation of interfaces in composites fabricated and stressed under realistic conditions. However, with the application of this method to reinforced polymers some problems arise both in the mathematical model for evaluating test data and in the practical performance of the test. Because in some cases the deformation of the relatively compliant polymeric matrices cannot be neglected, an extension of the existing model is required. For this purpose, the elastic energy of the material around the debonded part of the fibre is estimated and included in the energy-balance analysis. Because of the small diameter of the fibres usually used for reinforcing polymers, a test apparatus was designed which ensures a high positioning accuracy in the xy plane as well as in the z direction. In order to minimise thermal and mechanical influences, the microscope for fibre selection and the force sensor/indenter are directly connected together and the apparatus is designed to be stiff in all components. A solid-state bending joint guarantees very precise control of the axial movement. Three examples of the application of this easy-to-handle and low-cost test apparatus are presented briefly in the paper: assess fibre/matrix combinations, measures to improve the interfacial adhesion and the influence of water on the interface.
International and European dangerous substances and dangerous goods regulations refer to the standard ISO 10156 (1996). This standard includes a test method and a calculation procedure for the determination of the flammability of gases and gas mixtures in air. The substance indices for the calculation, the so called Tci values, which characterise the fire potential, are provided as well. These ISO Tci values are derived from explosion diagrams of older literature sources which do not take into account the test method and the test apparatus. However, since the explosion limits are influenced by apparatus parameters, the Tci values and lower explosion limits, given by the ISO tables, are inconsistent with those measured according to the test method of the same standard. In consequence, applying the ISO Tci values can result in wrong classifications. In this paper internationally accepted explosion limit test methods were evaluated and Tci values were derived from explosion diagrams. Therefore, an open vessel method with flame propagation criterion was favoured. These values were compared with the Tci values listed in ISO 10156. In most cases, significant deviations were found. A detailed study about the influence of inert gases on flammability is the objective of Part 2.