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Dive into the research topics where Velichka Kontozova-Deutsch is active.

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Featured researches published by Velichka Kontozova-Deutsch.


Talanta | 2011

Optimization of the ion chromatographic quantification of airborne fluoride, acetate and formate in the Metropolitan Museum of Art, New York

Velichka Kontozova-Deutsch; Felix Deutsch; László Bencs; Agnieszka Krata; René Van Grieken; Karolien De Wael

Ion chromatographic (IC) methods have been compared in order to achieve an optimal separation of fluoride, acetate and formate under various elution conditions on two formerly introduced analytical columns (i and ii) and a novel one (iii): (i) an IonPac AS14 (250 mm × 4 mm I.D.), (ii) Allsep A-2 (150 mm × 4.6mm I.D.), and (iii) an IC SI-50 4E (250 mm (length) × 4mm (internal diameter - I.D.)). The IC conditions for the separation of the anions concerned were optimized on the IC SI-50 4E column. A near baseline separation of these anions was attained on the IonPac AS14, whereas the peaks of fluoride and acetate could not be resolved on the Allsep A-2. A baseline separation for the three anions was achieved on the IC SI-50 4E column, when applying an eluent mixture of 3.2 mmol/L Na(2)CO(3) and 1.0 mmol/L NaHCO(3) with a flow rate of 1.0 mL/min. The highest precision of 1.7, 3.0 and 2.8% and the best limits of detection (LODs) of 0.014, 0.22 and 0.17 mg/L for fluoride, acetate and formate, respectively, were obtained with the IC SI-50 4E column. Hence, this column was applied for the determination of the acetic and formic acid contents of air samples taken by means of passive gaseous sampling at the Metropolitan Museum of Art in New York, USA. Atmospheric concentrations of acetic and formic acid up to 1050 and 450 μg/m(3), respectively, were found in non-aerated showcases of the museum. In galleries and outdoors, rather low levels of acetic and formic acid were detected with average concentrations of 50 and 10 μg/m(3), respectively. The LOD data of acetate and formate on the IC SI-50 4E column correspond to around 0.5 μg/m(3) for both acetic and formic acid in air samples.


Talanta | 2009

Single-run ion chromatographic separation of inorganic and low-molecular-mass organic anions under isocratic elution: Application to environmental samples

Agnieszka Krata; Velichka Kontozova-Deutsch; László Bencs; Felix Deutsch; René Van Grieken

For the isocratic ion chromatography (IC) separation of low-molecular-mass organic acids and inorganic anions three different anion-exchange columns were studied: IonPac AS14 (9 microm particle size), Allsep A-2 (7 microm particle size), and IC SI-50 4E (5 microm particle size). A complete baseline separation for all analyzed anions (i.e., F(-), acetate, formate, Cl(-), NO(2)(-), Br(-), NO(3)(-), HPO(4)(2-) and SO(4)(2-)) in one analytical cycle of shorter than 17 min was achieved on the IC SI-50 4E column, using an eluent mixture of 3.2mM Na(2)CO(3) and 1.0mM NaHCO(3) with a flow rate of 1.0 mL min(-1). On the IonPac AS14 column, it was possible to separate acetate from inorganic anions in one run (i.e., less than 9 min), but not formate, under the following conditions: 3.5mM Na(2)CO(3) plus 1.0mM NaHCO(3) with a flow rate of 1.2 mL min(-1). Therefore, it was necessary to adapt a second run with a 2.0mM Na(2)B(4)O(7) solution as an eluent under a flow rate of 0.8 mL min(-1) for the separation of organic ions, which considerably enlarged the analysis time. For the Allsep A-2 column, using an eluent mixture of 1.2mM Na(2)CO(3) plus 1.5mM NaHCO(3) with a flow rate of 1.6 mL min(-1), it was possible to separate almost all anions in one run within 25 min, except the fluoride-acetate critical pair. A Certified Multianion Standard Solution PRIMUS for IC was used for the validation of the analytical methods. The lowest RSDs (less than 1%) and the best LODs (0.02, 0.2, 0.16, 0.11, 0.06, 0.05, 0.04, 0.14 and 0.09 mg L(-1) for F(-), Ac(-), For(-), Cl(-), NO(2)(-), Br(-), NO(3)(-), HPO(4)(2-) and SO(4)(2-), respectively) were achieved using the IC SI-50 4E column. This column was applied for the separation of concerned ions in environmental precipitation samples such as snow, hail and rainwater.


Talanta | 2008

Efficient separation of acetate and formate by ion chromatography: application to air samples in a cultural heritage environment.

Velichka Kontozova-Deutsch; Agnieszka Krata; F. Deutsch; László Bencs; René Van Grieken

A method for the separation of acetate and formate anions by ion chromatography has been optimized under various measurement conditions (e.g. the composition of the mobile phase, and the flow rate of the eluent). For this purpose, two different analytical columns were examined: the IonPac AS14 (250 mm x 4 mm i.d.; designed mostly for the separation of inorganic anions) and the Allsep A-2 (150 mm x 4.6 mm i.d.; designed for the separation of low-molecular mass organic acids). However, nearly baseline separation of acetate and formate has been found on each column using the following conditions: (i) IonPac AS14 column and 2.0 mM Na2B4O7 solution as an eluent with a flow rate of 1.0 ml/min, or (ii) Allsep A-2 column and an eluent containing a mixture of 1.2 mM Na2CO3 plus 1.5 mM NaHCO3 with a flow rate of 1.3 ml/min. Additionally, the separation of fluoride from acetate and formate on both columns was studied. On the IonPac AS14 column it was possible to separate all three investigated anions. However, on the Allsep A-2 column, when the concentration of fluoride was comparable to, or higher than acetate, it was impossible to achieve good separation of these two anions, even using the optimized elution procedure. Therefore, the measurements of real samples were carried out with the use of IonPac AS14 column. The concentrations of acetate and formate have been determined in the air samples of the Cathedral of Cologne (Germany), after sampling the corresponding acids by passive diffusion tubes. Average concentrations of 122 and 9 microg/m(3) for acetic and formic acids were found, respectively, inside the Cathedral and in a depot with medieval stained glass panels.


Atmospheric Environment | 2009

Atmospheric BTEX-concentrations in an area with intensive street traffic

Anna J. Buczyńska; Agnieszka Krata; Marianne Stranger; Ana F. L. Godoi; Velichka Kontozova-Deutsch; László Bencs; Inge Naveau; Edward Roekens; René Van Grieken


Microchemical Journal | 2011

Evaluation of airborne particles at the Alhambra monument in Granada, Spain

Benjamin Horemans; Carolina Cardell; László Bencs; Velichka Kontozova-Deutsch; Karolien De Wael; René Van Grieken


Environmental Earth Sciences | 2011

Characterization of indoor and outdoor atmospheric pollutants impacting architectural monuments: the case of San Jerónimo Monastery (Granada, Spain).

Velichka Kontozova-Deutsch; Carolina Cardell; Maja Urosevic; E. Ruiz-Agudo; Felix Deutsch; René Van Grieken


Microchemical Journal | 2008

Monitoring of NO2 in the ambient air with passive samplers before and after a road reconstruction event

Marianne Stranger; Agnieszka Krata; Velichka Kontozova-Deutsch; László Bencs; F. Deutsch; Anna Worobiec; Inge Naveau; Edward Roekens; René Van Grieken


Microchemical Journal | 2008

A seasonal study of atmospheric conditions influenced by the intensive tourist flow in the Royal Museum of Wawel Castle in Cracow, Poland

Anna Worobiec; Lucyna Samek; Paweł Karaszkiewicz; Velichka Kontozova-Deutsch; Elzbieta Stefaniak; Katleen Van Meel; Agnieszka Krata; László Bencs; René Van Grieken


Mikrochimica Acta | 2008

Investigation of gaseous and particulate air pollutants at the Basilica Saint-Urbain in Troyes, related to the preservation of the medieval stained glass windows

Velichka Kontozova-Deutsch; Ricardo H. M. Godoi; Anna Worobiec; Zoya Spolnik; Agnieszka Krata; Felix Deutsch; René Van Grieken


Mikrochimica Acta | 2008

Application of EPMA and XRF for the investigation of particulate pollutants in the field of cultural heritage

Velichka Kontozova-Deutsch; Felix Deutsch; Ricardo H. M. Godoi; Zoya Spolnik; William Wei; René Van Grieken

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Felix Deutsch

Flemish Institute for Technological Research

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László Bencs

Hungarian Academy of Sciences

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Ricardo H. M. Godoi

Federal University of Paraná

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