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Sample preparation for testing

Sample preparation for tests in solutions 60pgmL water solution of moxifloxacin hydrochloride were measured off on quartz dishes of 4 cm diameter with the addition of water or of the appropriate water salt solution (CUSO4 5H2O, ZnS04-71120, Fe2(S04)3 -H20, Al2(S04)3 I8H2O). The dishes were sealed with a quartz lid. [Pg.241]

Sample preparation for tests in solid phase Samples were prepared by measuring off 60- J,g mL" methanol solution of moxifloxacin hydrochloride with the addition of water or the appropriate salt aqueous solution on Petri dishes of 5 cm diameter. Samples were mixed and evaporated in a water bath until dry matter was obtained. After irradiation, the content of individual dishes was dissolved in methanol. [Pg.242]

MRS has been found to be a useful technique to characterize raw materials and finished textile products. Because textile test specimens are in solid form, diffuse reflectance spectroscopy provides a special advantage by eliminating extensive sample preparation for testing textile materials such as fiber, yarn, and fabric. NIR analysis is useful because a sample may be rapidly tested without destroying its integrity. [Pg.486]

A8.8.1 No statement is made concerning either the precision or bias of Annex A8 for mass-percent water because the test method is used primarily for sample preparation for Test Method D 2892. [Pg.479]

High viscosities of polymers and different constants of diffusion and relaxation of components in oligomer and polymer blends are the factors which determine the difficulty of getting the equilibrium state of such systems which is attained at different velocities and at different structural levels. Therefore, the methods of sample preparation for testing and the conditions and duration of sample storage (i.e its prehistory) may affect the experimental results. This very circumstance may be the reason for the highly contradictory experimental data reported on the mutual solubility (compatibility) of components in polymer blends [129,162-166]. [Pg.28]

All six samples at both sites were prepared the same way. Five separate aliquots from each sample were separately sampled and prepared for testing. Each aliquot was then measured three times. Conditions and standard operating procedures for METHODS A and B were carefully specified for both Labs 1 and 2. [Pg.173]

Many of the heat-pressured samples prepared for the ZST test showed bubbles and discoloration. This is thought to be due to oligomers formed at the end of the polymerization when the reaction is pushed to high conversion. In... [Pg.83]

When round robin tests were performed to test the reproducibility of these standard procedures, large coefficients of variation between laboratories were obtained for tin-free paints (78-80% and 24-32% for the ISO and ASTM methods respectively Haslbeck and Holm, 2005). These discrepancies have multiple sources such as the analytical method (Haslbeck and Holm (2005) report 4-54% deviations when different laboratories measuring samples of known concentration), the sea water conditions both in the holding tank and the measuring tank (Haslbeck and Holm, 2005), the sample preparation for analysis... [Pg.213]

This chapter provides the novice and the experienced analyst with an overview of sample preparation techniques focusing on solid dosage forms. It describes the best practices in the dilute and shoot approach, and the tricks of the trade in grinding, mixing, sonication, dilution and filtration of drug products. Selected case studies of sample preparations for assays and impurity testing are used to illustrate the strategies, trade-offs... [Pg.123]

The sizing screen was cleaned with compressed air to remove any material lodged on its upper surface in preparation for testing next sample. [Pg.61]

The analysis of biomolecules by AFM is sometimes [3] referred to as surface biology, as opposed to the so-called test-tube biology, because the immobilisation of oligonucleotides on sohd surfaces is central to the design, fabrication and operation of DNA-based microdevices, such as biosensors, DNA micro- and nanoarrays, microPCR and lab-on-a-chip devices. As the analysed biomolecules are in close contact and very often in intimate interaction with the surface, sample preparation for the AFM analysis of surface-immobihsed biomolecules is both critical and dehcate. The biomolecules need to be firmly anchored on the substrate, which has to have a sufficiently minimal or easily discriminated topography [1]. The Kleinschmidt method [6] for the DNA... [Pg.123]

Laboratory sample. A sample, intended for testing or analysis, prepared from a gross sample or otherwise obtained. The laboratory sample must retain the composition of the gross sample. Often reduction in particle size is necessary in the course of reducing the quantity. [Pg.48]

Appreciation is expressed to the following MFPUL employees Dr. A. L. Wooten (retired) for resin synthesis Gary Stovall and George Miller for resin and flake board sample preparation and testing and Lynn Prewitt for GFC work. Materials were donated in support of this project by Borden... [Pg.335]

Intermediate Precision. Intermediate precision expresses within-laboratory variation and is generally performed on different days using different analysts, equipment, and sample preparations. This test may not be applicable if the laboratory has only one workstation. Additionally, this test may not be appropriate for automated workstations that are operating under the same environment and controls within a laboratory. This assumption is made on the basis that the automated workstations are identical (i.e., same configuration, same software and hardware) and that they have been suitably qualified and maintained to a consistent standard and operate under a similar climatic environment. The influence of the analyst is reduced to the preparation of solvents, and this should be covered by the robustness studies. [Pg.76]

The overall penetration depth, and therefore the measured hardness, depend on the time of load action on the tester and also on the technique of preparing the sample surface for test. [Pg.218]

Ivermectin (IVER) is a drug with a broad spectrum of activity against gastrointestinal nematodes and lung parasites in food-producing animals. In the EU, the maximum residue levels set for IVER in the liver of sheep, pigs, and cattle are 15,15, and 100 tg/kg, respectively (217). The use of automated SPE equipment was described for IVER HPLC analysis in animal liver samples. This automated system, ASPEC, was used for the SPE purification step in order to provide more efficient and faster sample preparation. Some tests were performed to obtain recovery and repeatability data. The mean recovery for spiked samples was more than 90% in the concentration range of 7.5-30 tg/kg. [Pg.679]

Iron Dilute 1 mL of the solution (100-mg sample) prepared for the Chloride test (above) to 40 mL with water. Add about 30 mg of ammonium persulfate crystals and 10 mL of ammonium thiocyanate TS. Any resulting red color does not exceed in intensity that produced by 2.0 mL of Iron Standard Solution (20 xg Fe) (see Solutions and Indicators) in an equal volume of a solution containing the same quantities of the reagents used in the test. [Pg.462]


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See also in sourсe #XX -- [ Pg.104 ]




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