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dc.contributor.authorHovde, Gunnhild
dc.date.accessioned2015-05-22T08:40:10Z
dc.date.accessioned2015-05-26T11:37:20Z
dc.date.available2015-05-22T08:40:10Z
dc.date.available2015-05-26T11:37:20Z
dc.date.issued2013
dc.identifier.citationNofima rapportserie. 32 p. Nofima, 2013
dc.identifier.isbn978-82-8296-077-9
dc.identifier.urihttp://hdl.handle.net/11250/284039
dc.description-
dc.description.abstractThe aim of this project is to validate Nofima BioLab’s method for analysis of soluble phosphorus. The definition of soluble phosphorus in this context is phosphorus that is not bound in bone material. Validating a method means investigating and establishing the method’s quality parameters. The tested method parameters will include recovery, bias, precision, ruggedness, limit of detection, limit of quantification, and uncertainty. The recovery test/spiking showed how important it is to have knowledge about the properties of the phosphate salts, especially the solubility. The repeatability of the method is similar to the repeatability of the well-established method for analysis of total phosphorus (ISO 6491). The combined measurement uncertainty of the method is low where the largest uncertainty contribution comes from diluting the sample.
dc.language.isoeng
dc.relation.urihttps://nofimaas.sharepoint.com/sites/public/_layouts/15/guestaccess.aspx?guestaccesstoken=tCubwE6KucpU6q2LlhC48UFz4DGVBzGDe%2fDtFlDUoM4%3d&docid=08feaf7c9a6274aacbb318b56b9849ea7
dc.titleValidation of a method for analysis of soluble phosphorus by use of alkaline extraction and spectrophotometric determination
dc.typeResearch report
dc.date.updated2015-05-22T08:40:10Z
dc.identifier.cristin1045285
dc.relation.projectEgen institusjon: 21149
dc.relation.projectEgen institusjon: 10167


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