排序方式: 共有51条查询结果,搜索用时 15 毫秒
1.
do Nascimento Ticiano Gomes Borges Arthur Luy Tavares Ferreira de Almeida Lara Mendes Ribeiro Êurica Adélia Nogueira Silva Fernanda Geny Calheiros da Costa Silva Valdemir do Nascimento Prata Ana Paula Basílio-Júnior Irinaldo Diniz Goulart Marília Oliveira Fonseca Morilla Demetrius Peireira de Freitas Johnnatan Duarte Aragão Cícero Flávio Soares 《Journal of Thermal Analysis and Calorimetry》2022,147(21):11949-11963
Journal of Thermal Analysis and Calorimetry - This work prepared and characterized microcapsule of Uncaria tomentosa (UT) in order to standardize a spray-dryer Uncaria tomentosa extract. The UT... 相似文献
2.
Fernando Coelho Demetrius VeroneseElizandra C.S Lopes Rodrigo C Rossi 《Tetrahedron letters》2003,44(30):5731-5735
In this communication we describe an easy and straightforward alternative method for the preparation of 3,4-substituted isoquinolin-1(2H)-ones, using Baylis-Hillman adducts as starting material. 相似文献
3.
Demetrius C. Levendis Jan C. A. Boeyens Eberhard W. Neuse 《Journal of chemical crystallography》1982,12(6):493-506
Crystalline biruthenocene is disordered at room temperature. The apparent symmetry ofP21
c applies to an average structure only. Better resolution is achieved by refinement in the space groupP1. The room-temperature X-ray structure, as refined in both space groups, shows that the mutual orientation of cyclopentadienyl rings within a sandwich is not conformationally important and that it depends on intermolecular interactions. 相似文献
4.
Ferrocene and nickelocene have pseudo-isomorphous structures at room temperature but only ferrocene undergoes a second-order phase transformation on cooling. Calculation and analysis of appropriate lattice-energy surfaces as a function of concerted ring rotation showed that ferrocene has a disordered structure at room temperature different from nickelocene which exhibits a single minimum in the lattice-energy function. The results readily suggest a mechanism for the ferrocene phase transformation. The correct low-temperature structure is predicted only after taking intramolecular interactions into account. 相似文献
5.
6.
Paraskevas D. Tzanavaras Demetrius G. Themelis Fotini S. Kika 《Central European Journal of Chemistry》2007,5(1):1-12
The present study reviews more than twenty years (1985-present) of published research on the development and application of
analytical procedures for the determination of chlorine dioxide, a widely used disinfectant and bleaching agent. The review
covers a variety of techniques including batch and automated spectrophotometry and fluorimetry, electroanalysis and chromatography.
The analytical figures of merit to the methods are presented, while critical discussion regarding their advantages and disadvantages
is addressed.
相似文献
7.
Paraskevas D. Tzanavaras Demetrius G. Themelis Anastasios Economou Georgios Theodoridis 《Mikrochimica acta》2003,142(1-2):55-62
Two new simple and rapid methods are reported for the accurate and precise spectrophotometric determination of captopril
(CPL) using flow (FI) and sequential injection (SI) analysis. The methods are based on the fast oxidation of CPL by Fe(III).
The produced Fe(II) reacts with 2,2′-dipyridyl-2-pyridylhydrazone (DPPH) in acidic medium to form a colored complex which
is monitored spectrophotometrically at 535 nm. Both methods allow the determination of the analyte up to 1000 mg L−1 at a sampling rate of 120 and 60 injections per hour for FI and SI, respectively. The methods are very precise [s
r=0.8 and 1.2% at 500 mg L−1 CPL (n=12) for FI and SI, respectively] and the 3σ detection limits (c
L=4.0 and 7.0 mg L1, respectively) are quite satisfactory. Their application to a variety of anti-hypertensive commercial pharmaceutical formulations
showed excellent results (relative errors, e
r, < ± 1.6% in all cases compared to an official HPLC method), while common pharmaceutical excipients were found not to interfere.
Recovery experiments further verified the accuracy of the developed methods, as the percent recoveries were in the range of
98.1–102.5%.
Author for correspondence. E-mail: themelis@chem.auth.gr
Received May 9, 2002; accepted January 8, 2003
Published online May 5, 2003 相似文献
8.
The present study reports the development and validation of a high-throughput high-performance liquid chromatographic (HPLC) assay for the determination of caffeine in food samples. The analyte was separated rapidly from sample matrix using a short monolithic column (50 mm × 4.6 mm i.d.). The flow rate was 3.0 mL min−1, while the mobile phase consisted of ACN/water (10:90, v/v). Caffeine was detected directly at 274 nm. Under the optimal HPLC conditions, the sampling rate was 60 h−1. The assay was validated for linearity, LOD and LOQ, precision, selectivity and ruggedness. The case of external calibration versus standard addition for the analysis of real samples was also examined. The proposed assay was applied to the analysis of beverages and coffee samples. 相似文献
9.
Paraskevas D. Tzanavaras Theano D. Karakosta Pantelis G. Rigas Demetrius G. Themelis Anastasia Zotou 《Central European Journal of Chemistry》2012,10(5):1459-1463
The first HPLC method for the separation of three paraben preservatives (methyl-, ethyl- and propyl parabens) using a core-shell analytical column is reported in this study. The separation was completed in less than 8 min at a low flow rate of 0.4 mL min−1 and an isocratic mobile phase containing 20% acetonitrile as organic modifier. The backpressure was < 200 bar in all cases, enabling the usage of conventional HPLC equipment. The proposed analytical procedure was validated for linearity (0.5–20 μg L−1), limits of detection (15–43 μg L−1) and quantification (50–142 μg L−1), selectivity, within day (1.3–1.5%) and day-to-day (3.4–4.6%) precision and accuracy. The proposed method has been applied to the determination of the selected paraben preservatives in commercially available hygiene wipes. The mean percent recoveries were found to be in the range of 98.0–98.4%. 相似文献
10.
Demetrius G. Themelis Sophia C. Karastogianni Paraskevas D. Tzanavaras 《Analytica chimica acta》2009,632(1):93-116
A highly selective sequential injection (SI) method for the automated determination of weak-acid-dissociable cyanides is reported. The analytical procedure is based on the on-line reaction of the analyte with ninhydrin in carbonate medium to form a coloured product (λmax = 510 nm). Cyanides are removed from sample matrix by acidification through a gas-diffusion step incorporated in the SI manifold. The effect of instrumental and chemical variables was studied. By adopting an on-line standard addition protocol, the sensitivity of the proposed method was enhanced drastically, without affecting the determination range. The assay was validated in terms of linearity (up to 200 μg L−1), limit of detection (cL = 2.5 μg L−1), limit of quantitation (cQ = 7.5 μg L−1), precision (sr < 2.5% at 100 μg L−1) and selectivity. High tolerance against critical species such as sulfides and thiocyanates was achieved. The applicability of the method was demonstrated by analyzing tap and mineral water samples at levels below the limits established by international E.U. and U.S. organizations. The percent recoveries were satisfactory in all cases, ranging between 94.2 and 103.6%. 相似文献