BS EN ISO 10993-15-2009 Biological evaluation of medical devices - Part 15 Identification and quantification of degradation nproducts from metals and alloys (ISO 10993-15 2000)《医疗器.pdf
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1、 , b) ratio of the exposed surface area of the sample to the volume of the electrolyte;c) composition and pH (with an uncertainty of Gb1 0,1) of the electrolyte and a description of the natural or referenceelectrode for the electrochemical test;d) composition and initial and final pH of the electrol
2、yte for the immersion test;e) temperature of the electrolyte;f) current density vs. potential curve(s), optionally the log (current density) vs. potential curve for comparison;g) open-circuit potential;h) breakdown potential Epand the current density at the breakdown potential;i) sweep rate;j) curre
3、nt density vs. time curve(s) and total test time;k) brief comments on the curves (e.g. hysteresis, peaks);l) description of any significant changes of the sample surface and/or of the electrolyte;m) results of analysis of degradation elements in the electrolyte, including degradation rate, reported
4、inmicrograms per square centimetre per hour (G6dg/cm2/h) for the electrostatic test or per seven days(G6dg/cm2/7 days) for the immersion test;n) method of chemical analysis of electrolyte;o) type of reference electrode all potentials should be referenced to the normal hydrogen electrode (NHE);p) nam
5、e of investigator;q) date(s) of investigation;r) signature of the investigator.BS EN ISO 10993-15:2009ISO 10993-15:2000(E) ISO 2000 All rights reserved 9Annex A(informative)Schematic diagram of the electrochemical measuring circuitKey1 Potentiostat2 Potential measurement3 Current measurement4 Workin
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