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41.
Ignacio López-García Mateo Sánchez-Merlos Manuel Hernández-Córdoba 《Spectrochimica Acta Part B: Atomic Spectroscopy》1997,52(14):378-2092
A graphite furnace atomic absorption spectrometric procedure for the determination of mercury is presented, in which the samples are suspended in a solution containing hydrofluoric and nitric acids. Silver nitrate (4% m/v) and potassium permanganate (3%) are incorporated, in the order specified, and aliquots are directly introduced into the graphite furnace. A fast heating programme with no conventional pyrolysis step is used. The detection limit for mercury in a 125 mg ml−1 suspension is 0.1 μg g−1. Calibration is performed by using aqueous standards. The reliability of the procedure is proved by analysing certified reference materials. 相似文献
42.
《Arabian Journal of Chemistry》2022,15(1):103472
As a representative of traditionally fermented Chinese medicine, Massa Medicata Fermentata (MMF) shows the functions of invigorating the spleen and stomach and promoting digestion, which plays an important role in the treatment of gastrointestinal diseases. The fermentation mechanism and the key factors that affect the quality of MMF have not been revealed yet, which has become an urgent issue that limits its clinical application. This article aims to systematically and comprehensively reveal the transformation of physical properties and the dynamic trend of chemical components including substrate components, volatile components, and lactic acid as anaerobic fermentation product during MMF fermentation. Along with obvious hyphae growth observed for MMF, the weight of MMF decreased, and the moisture and temperature increased. Through the quantified 14 components from substrate, ferulic acid increased from 45.53 ± 6.94 to 141.89 ± 78.40 μg/g, while glycosides and phenolic acids declined except caffeic acid. Also, within the 66 volatile components analyzed, alcohols and acids increased, while aldehydes and ketones decreased. Lactic acid was not detected in the fermentation substrate, but an apparent increase in lactic acid content was observed along with the increased fermentation days, resulting in 2.54 ± 0.15 mg/g on day 8. Based on the tested components, the fermentation process of MMF was discriminated into three distinct stages by principal component analysis, and an optimal fermentation time of four days was proposed. The results of this study will be of great significance to clarify the characteristics of fermentation and conduce to improving quality standards of MMF. 相似文献
43.
Manganese in vitamin-minerals tablets was determined by solid sampling electrothermal atomic absorption spectrometry (SS-ETAAS) using three different calibration methods, namely calibration against aqueous standards, standard addition with aqueous standards on solid samples and calibration against solid certified standards. Samples were only finely ground and introduced directly into the furnace by means of solid autosampler system without any dissolving process. Effects of different calibration techniques, temperatures and heating rates of atomization and pyrolysis steps on the accuracy and precision of the analyte elements were investigated. After optimization of the experimental parameters, there is good agreement (at 95% confidence level) between the results obtained by solid sampling and those obtained by acid digestion of samples. 相似文献
44.
45.
Summary Dynamic headspace and simultaneous steam distillation-extraction techniques were used to isolate volatile components of Parmesan cheese. Identification of the substances was carried out by GC and GC-MS; 110 compounds were identified in the samples obtained using the headspace technique, 105 in the extracts; among them, about 50 compounds were isolated with both procedures. Mass spectral data showed evidence for a number of newly reported compounds such as 3-(methylthio)propanal, -tetradecalactone, 9-tetra-decenoic and 9-hexadecenoic acids. Mass spectra of some compounds are discussed and a comparison between the results obtained with the two sampling methods is given. 相似文献
46.
The expression of the continuous distribution function F(x) is obtained whenever % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqefm0B1jxALjhiov2D% aebbfv3ySLgzGueE0jxyaibaiGc9yrFr0xXdbba91rFfpec8Eeeu0x% Xdbba9frFj0-OqFfea0dXdd9vqaq-JfrVkFHe9pgea0dXdar-Jb9hs% 0dXdbPYxe9vr0-vr0-vqpWqaaeaabiGaciaacaqabeaadaqaaqGaaO% qaaerbhv2BYDwAHbacfiGaa8xBaiaabIcacaWG4bGaaiilaiaadMha% caqGPaGaa8hiaiaab2dacaWFGaGaa8xraiaa-HcacaWFybGaa8hiai% aa-XhacaWFGaGaa8hEaiaa-bcacqGHKjYOcaWFGaGaa8hwaiaa-bca% cqGHKjYOcaWFGaGaa8xEaiaa-Lcaaaa!53EE!\[m{\rm{(}}x,y{\rm{)}} {\rm{ = }} E(X | x \le X \le y)\]is known. Moreover, we obtain the necessary and sufficient conditions so that any function m: 2 is the conditional expectation % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqefm0B1jxALjhiov2D% aebbfv3ySLgzGueE0jxyaibaiGc9yrFr0xXdbba91rFfpec8Eeeu0x% Xdbba9frFj0-OqFfea0dXdd9vqaq-JfrVkFHe9pgea0dXdar-Jb9hs% 0dXdbPYxe9vr0-vr0-vqpWqaaeaabiGaciaacaqabeaadaqaaqGaaO% qaaiaadweacaGGOaGaamiwaerbhv2BYDwAHbacfiGaa8hiaiaacYha% caWFGaGaa8hEaiaa-bcacqGHKjYOcaWFGaGaa8hwaiaa-bcacqGHKj% YOcaWFGaGaa8xEaiaacMcaaaa!4D0D!\[E(X | x \le X \le y)\]of a random variable X with continuous distribution function. Furthermore, we relate m(x,y) to order statistics. 相似文献
47.
For the major, minor and trace element analysis of the inorganic compounds of a Ruhr-Saar coal different preparation techniques are investigated with X-ray fluorescence analysis, electron microprobe and classical wet chemical methods minimizing sample weight at standard preparation times and analytical accuracies. Considering accuracy as well as preparation efforts, determinations by electron microprobe on small sample amounts (<50 mg) proved to be superior to the other methods.Abbreviations AAS
atomic absorbtion spectrometry
- EMA
electron microprobe analysis
- IC
ion chromatography
- ISE
ion sensitive electrode
- PHOT
photometry
- WCA
wet chemical analysis
- XRF
X-ray fluorescence analysis
- LTA
low temperature plasma ashing
- HTA
high temperature ashing
- l.o.i.
loss on ignition 相似文献
48.
H. G. Struppe F. Franke J. Hofmann B. Ondruschka 《Journal of chromatography. A》1996,750(1-2):239-244
In contrast to usability of Curie-point pyrolysis at 700°C directly attached to gas chromatography-mass spectrometry (GC-MS) for determination of organic wood preservatives in waste wood samples the investigation method reported here consists of thermal desorption at temperatures about 260°C in connection with GC-MS for peak identification or GC with flame ionization detection for quantitative analyses. So-called “modified closeable sampling columns” are used as batch-reactor in thermal desorption experiments. Desorbed vapours can be introduced on capillary columns without sample discrimination and without a disturbing lost of resolution. In this manner a lot of individual polycyclic aromatic hydrocarbons were determinated in waste wood samples, especially in railway sleepers. 相似文献
49.
A new reactor and a novel in-situ sampling technique were developed for the study of the synthesis of CeO2 powders produced from dissolved cerium nitrate salts. The conical reactor minimized particle recirculation and provided a
highly symmetrical and undisturbed plasma flow suitable for the analysis of the phenomena affecting the formation of CeO2 powders. Both a calorimetric study of the reactor and a thermodynamic analysis of CeO2 formation were conducted. The sampling probe is described and near-isokinetic sampling was achieved. The sampled particles
were collected using a miniature wet collection system, i.e. a mist atomizer and a custom-made spray chamber. A numerical
simulation of the velocity and temperature fields of the plasma gas in the reactor was done using Fluent. A comprehensive
droplet-to-particle formation mechanism presented elsewhere is revisited and expanded based on calorimetry, thermodynamics
of CeO2 formation, numerical simulations and collected particles. No traces of other oxidation states other than CeO2 were found. 相似文献
50.
用环形扩散管和滤纸联用采样技术采集空气中氨和铵盐 总被引:1,自引:0,他引:1
建立了环形扩散管和滤纸采样夹联用,分形态同时采集空气中所态氨和颗粒态铵盐的方法。在同一气流中,采用涂渍1.5%草酸乙醇水溶液的环形扩散管采集气态氨,用浸渍上述试剂的玻璃纤维纸和慢速定量滤纸分别采集颗粒安和第一层滤纸上的铵盐挥发产生的氨气。用靛酚蓝比色法分别测定氨和铵盐。当采气流速为1.0L/min时,采样效率高于98.2%。将本法测得的氨气和铵盐的总量与标准采样方法的测定结果比较。无显著性差异(P 相似文献