Petrović, Srđan

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orcid::0000-0003-4763-904X
  • Petrović, Srđan (4)
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Author's Bibliography

Detection Limit for an Adsorption-Based Mercury Sensor

Sarajlić, Milija; Đurić, Zoran G.; Jović, Vesna; Petrović, Srđan; Đorđević, Dragana

(Elsevier, 2013)

TY  - JOUR
AU  - Sarajlić, Milija
AU  - Đurić, Zoran G.
AU  - Jović, Vesna
AU  - Petrović, Srđan
AU  - Đorđević, Dragana
PY  - 2013
UR  - https://dais.sanu.ac.rs/123456789/378
AB  - A novel readout procedure for the determination of detection limit at an adsorption-based mercury sensor is described. The procedure is based on the evaluation of the initial voltage slope in time evolution of adsorbed elementary mercury. The Langmuir time-dependent adsorption theory is utilized to derive it. This procedure gives the theoretical minimum for the detection for this type of the sensor, which is estimated at 180 ng/m3. This is five times lower than the best previously reported results. This procedure can also be used for regular sensor readout. This work describes the experimental procedure for mercury sensor fabrication as well as its measurement cycle. The sensor is working in the cycles of mercury adsorption and evaporation induced by heating. It is shown that every part of the cycle can be monitored by measuring output voltage of the sensor without any additional measurements like surface temperature or rate of the evaporation.
PB  - Elsevier
T2  - Microelectronic Engineering
T1  - Detection Limit for an Adsorption-Based Mercury Sensor
SP  - 118
EP  - 122
VL  - 103
DO  - 10.1016/j.mee.2012.10.009
UR  - https://hdl.handle.net/21.15107/rcub_dais_378
ER  - 
@article{
author = "Sarajlić, Milija and Đurić, Zoran G. and Jović, Vesna and Petrović, Srđan and Đorđević, Dragana",
year = "2013",
abstract = "A novel readout procedure for the determination of detection limit at an adsorption-based mercury sensor is described. The procedure is based on the evaluation of the initial voltage slope in time evolution of adsorbed elementary mercury. The Langmuir time-dependent adsorption theory is utilized to derive it. This procedure gives the theoretical minimum for the detection for this type of the sensor, which is estimated at 180 ng/m3. This is five times lower than the best previously reported results. This procedure can also be used for regular sensor readout. This work describes the experimental procedure for mercury sensor fabrication as well as its measurement cycle. The sensor is working in the cycles of mercury adsorption and evaporation induced by heating. It is shown that every part of the cycle can be monitored by measuring output voltage of the sensor without any additional measurements like surface temperature or rate of the evaporation.",
publisher = "Elsevier",
journal = "Microelectronic Engineering",
title = "Detection Limit for an Adsorption-Based Mercury Sensor",
pages = "118-122",
volume = "103",
doi = "10.1016/j.mee.2012.10.009",
url = "https://hdl.handle.net/21.15107/rcub_dais_378"
}
Sarajlić, M., Đurić, Z. G., Jović, V., Petrović, S.,& Đorđević, D.. (2013). Detection Limit for an Adsorption-Based Mercury Sensor. in Microelectronic Engineering
Elsevier., 103, 118-122.
https://doi.org/10.1016/j.mee.2012.10.009
https://hdl.handle.net/21.15107/rcub_dais_378
Sarajlić M, Đurić ZG, Jović V, Petrović S, Đorđević D. Detection Limit for an Adsorption-Based Mercury Sensor. in Microelectronic Engineering. 2013;103:118-122.
doi:10.1016/j.mee.2012.10.009
https://hdl.handle.net/21.15107/rcub_dais_378 .
Sarajlić, Milija, Đurić, Zoran G., Jović, Vesna, Petrović, Srđan, Đorđević, Dragana, "Detection Limit for an Adsorption-Based Mercury Sensor" in Microelectronic Engineering, 103 (2013):118-122,
https://doi.org/10.1016/j.mee.2012.10.009 .,
https://hdl.handle.net/21.15107/rcub_dais_378 .
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An adsorption-based mercury sensor with continuous readout

Sarajlić, Milija; Đurić, Zoran G.; Jović, Vesna; Petrović, Srđan; Đorđević, Dragana

(Springer-Verlag, 2013)

TY  - JOUR
AU  - Sarajlić, Milija
AU  - Đurić, Zoran G.
AU  - Jović, Vesna
AU  - Petrović, Srđan
AU  - Đorđević, Dragana
PY  - 2013
UR  - https://dais.sanu.ac.rs/123456789/377
AB  - A novel readout procedure for a mercury sensor has been proposed. The sensor is based on the surface adsorption. Mercury vapor is adsorbed at the surface of a thin gold layer patterned into four meanders which are connected into a Wheatstone bridge configuration. Sensing is achieved by the resistivity change of the gold film during mercury adsorption. Direct output from the sensor is electric voltage. It takes an additional procedure to convert voltage to mercury concentration. This type of sensor is improved by introducing continuous readout procedure for the voltage–concentration conversion. By using this readout procedure it is possible to monitor mercury vapor concentration as a function of time. Readout is based on the Langmuir time–dependent adsorption theory. This paper illustrates a practical implementation of the new readout procedure.
PB  - Springer-Verlag
T2  - Microsystem Technologies
T1  - An adsorption-based mercury sensor with continuous readout
SP  - 749
EP  - 755
VL  - 19
IS  - 5
DO  - 10.1007/s00542-012-1679-6
UR  - https://hdl.handle.net/21.15107/rcub_dais_377
ER  - 
@article{
author = "Sarajlić, Milija and Đurić, Zoran G. and Jović, Vesna and Petrović, Srđan and Đorđević, Dragana",
year = "2013",
abstract = "A novel readout procedure for a mercury sensor has been proposed. The sensor is based on the surface adsorption. Mercury vapor is adsorbed at the surface of a thin gold layer patterned into four meanders which are connected into a Wheatstone bridge configuration. Sensing is achieved by the resistivity change of the gold film during mercury adsorption. Direct output from the sensor is electric voltage. It takes an additional procedure to convert voltage to mercury concentration. This type of sensor is improved by introducing continuous readout procedure for the voltage–concentration conversion. By using this readout procedure it is possible to monitor mercury vapor concentration as a function of time. Readout is based on the Langmuir time–dependent adsorption theory. This paper illustrates a practical implementation of the new readout procedure.",
publisher = "Springer-Verlag",
journal = "Microsystem Technologies",
title = "An adsorption-based mercury sensor with continuous readout",
pages = "749-755",
volume = "19",
number = "5",
doi = "10.1007/s00542-012-1679-6",
url = "https://hdl.handle.net/21.15107/rcub_dais_377"
}
Sarajlić, M., Đurić, Z. G., Jović, V., Petrović, S.,& Đorđević, D.. (2013). An adsorption-based mercury sensor with continuous readout. in Microsystem Technologies
Springer-Verlag., 19(5), 749-755.
https://doi.org/10.1007/s00542-012-1679-6
https://hdl.handle.net/21.15107/rcub_dais_377
Sarajlić M, Đurić ZG, Jović V, Petrović S, Đorđević D. An adsorption-based mercury sensor with continuous readout. in Microsystem Technologies. 2013;19(5):749-755.
doi:10.1007/s00542-012-1679-6
https://hdl.handle.net/21.15107/rcub_dais_377 .
Sarajlić, Milija, Đurić, Zoran G., Jović, Vesna, Petrović, Srđan, Đorđević, Dragana, "An adsorption-based mercury sensor with continuous readout" in Microsystem Technologies, 19, no. 5 (2013):749-755,
https://doi.org/10.1007/s00542-012-1679-6 .,
https://hdl.handle.net/21.15107/rcub_dais_377 .
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LaMO3 (M = Mg, Ti, Fe) perovskite type oxides: Preparation, characterization and catalytic properties in methane deep oxidation

Petrović, Srđan; Terlecki Baričević, Ana; Karanović, Ljiljana; Kirilov-Stefanov, Plamen; Zdujić, Miodrag; Dondur, Vera; Paneva, D.; Mitov, I.; Rakić, V.

(Elsevier, 2008)

TY  - JOUR
AU  - Petrović, Srđan
AU  - Terlecki Baričević, Ana
AU  - Karanović, Ljiljana
AU  - Kirilov-Stefanov, Plamen
AU  - Zdujić, Miodrag
AU  - Dondur, Vera
AU  - Paneva, D.
AU  - Mitov, I.
AU  - Rakić, V.
PY  - 2008
UR  - https://dais.sanu.ac.rs/123456789/3586
AB  - Two new series of perovskite-type oxides LaMO3 (M = Mg, Ti, Fe) with different ratio Mg/Fe (MF) and Ti/Fe (TF) in the B cation site were prepared by annealing the precursor, obtained by the mechanochemical activation (MCA) of constituent metal oxides, at 1000 °C in air. In addition, two closely related perovskites LaFeO3 (LF) and LaTi0.5Mg0.5O3 (TM (50:50)) were synthesized in the similar way. Using MCA method, perovskites were obtained in rather short time and at room temperature. The samples were characterized by X-ray powder diffraction (XRPD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS), temperature programmed desorption of oxygen (TPD), Mössbauer spectroscopy, BET surface area measurements and tested in methane deep oxidation. According to XRPD analysis all synthesized samples are almost single perovskite phase, with trace amounts of La2O3 phase. Data of Mössbauer spectroscopy identify Fe3+ in octahedral coordination. The activity of perovskite in methane deep oxidation increases in the order TM (50:50) < MF series < TF series. Higher activity of TF samples in respect to MF with similar Fe content can be related to the structural characteristic, mainly to the presence of predominantly most labile oxygen species evidenced by TPD at lowest temperature of oxygen evaluation. In used experimental conditions, the Fe substituted perovskite are thermal stable up to the temperature of 850 °C. The stability of Fe active sites is probably the most important parameter responsible for thermal stability of perovskite, but the atomic surface composition also should be taken into account. © 2007 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Applied Catalysis B: Environmental
T1  - LaMO3 (M = Mg, Ti, Fe) perovskite type oxides: Preparation, characterization and catalytic properties in methane deep oxidation
SP  - 186
EP  - 198
VL  - 79
IS  - 2
DO  - 10.1016/j.apcatb.2007.10.022
UR  - https://hdl.handle.net/21.15107/rcub_dais_3586
ER  - 
@article{
author = "Petrović, Srđan and Terlecki Baričević, Ana and Karanović, Ljiljana and Kirilov-Stefanov, Plamen and Zdujić, Miodrag and Dondur, Vera and Paneva, D. and Mitov, I. and Rakić, V.",
year = "2008",
abstract = "Two new series of perovskite-type oxides LaMO3 (M = Mg, Ti, Fe) with different ratio Mg/Fe (MF) and Ti/Fe (TF) in the B cation site were prepared by annealing the precursor, obtained by the mechanochemical activation (MCA) of constituent metal oxides, at 1000 °C in air. In addition, two closely related perovskites LaFeO3 (LF) and LaTi0.5Mg0.5O3 (TM (50:50)) were synthesized in the similar way. Using MCA method, perovskites were obtained in rather short time and at room temperature. The samples were characterized by X-ray powder diffraction (XRPD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS), temperature programmed desorption of oxygen (TPD), Mössbauer spectroscopy, BET surface area measurements and tested in methane deep oxidation. According to XRPD analysis all synthesized samples are almost single perovskite phase, with trace amounts of La2O3 phase. Data of Mössbauer spectroscopy identify Fe3+ in octahedral coordination. The activity of perovskite in methane deep oxidation increases in the order TM (50:50) < MF series < TF series. Higher activity of TF samples in respect to MF with similar Fe content can be related to the structural characteristic, mainly to the presence of predominantly most labile oxygen species evidenced by TPD at lowest temperature of oxygen evaluation. In used experimental conditions, the Fe substituted perovskite are thermal stable up to the temperature of 850 °C. The stability of Fe active sites is probably the most important parameter responsible for thermal stability of perovskite, but the atomic surface composition also should be taken into account. © 2007 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Applied Catalysis B: Environmental",
title = "LaMO3 (M = Mg, Ti, Fe) perovskite type oxides: Preparation, characterization and catalytic properties in methane deep oxidation",
pages = "186-198",
volume = "79",
number = "2",
doi = "10.1016/j.apcatb.2007.10.022",
url = "https://hdl.handle.net/21.15107/rcub_dais_3586"
}
Petrović, S., Terlecki Baričević, A., Karanović, L., Kirilov-Stefanov, P., Zdujić, M., Dondur, V., Paneva, D., Mitov, I.,& Rakić, V.. (2008). LaMO3 (M = Mg, Ti, Fe) perovskite type oxides: Preparation, characterization and catalytic properties in methane deep oxidation. in Applied Catalysis B: Environmental
Elsevier., 79(2), 186-198.
https://doi.org/10.1016/j.apcatb.2007.10.022
https://hdl.handle.net/21.15107/rcub_dais_3586
Petrović S, Terlecki Baričević A, Karanović L, Kirilov-Stefanov P, Zdujić M, Dondur V, Paneva D, Mitov I, Rakić V. LaMO3 (M = Mg, Ti, Fe) perovskite type oxides: Preparation, characterization and catalytic properties in methane deep oxidation. in Applied Catalysis B: Environmental. 2008;79(2):186-198.
doi:10.1016/j.apcatb.2007.10.022
https://hdl.handle.net/21.15107/rcub_dais_3586 .
Petrović, Srđan, Terlecki Baričević, Ana, Karanović, Ljiljana, Kirilov-Stefanov, Plamen, Zdujić, Miodrag, Dondur, Vera, Paneva, D., Mitov, I., Rakić, V., "LaMO3 (M = Mg, Ti, Fe) perovskite type oxides: Preparation, characterization and catalytic properties in methane deep oxidation" in Applied Catalysis B: Environmental, 79, no. 2 (2008):186-198,
https://doi.org/10.1016/j.apcatb.2007.10.022 .,
https://hdl.handle.net/21.15107/rcub_dais_3586 .
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Catalytic combustion of methane over Pd containing perovskite type oxides

Petrović, Srđan; Karanović, Ljiljana; Stefanov, Plamen K.; Zdujić, Miodrag; Terlecki Baričević, Ana

(Elsevier Science Bv, Amsterdam, 2005)

TY  - JOUR
AU  - Petrović, Srđan
AU  - Karanović, Ljiljana
AU  - Stefanov, Plamen K.
AU  - Zdujić, Miodrag
AU  - Terlecki Baričević, Ana
PY  - 2005
UR  - https://dais.sanu.ac.rs/123456789/4838
AB  - The mixed perovskite type oxides with nominal formula LaTi0.5Mg0.5-xPdxO3, (0  LT = x  LT = 0.10) were prepared by anneling the ethanol solution of precursor in nitrogen flow at 1200 degrees C. X-ray powder diffraction (XRPD) analysis shows that the orthorhombic perovskite structure was found in all investigated samples. However, at least a part of palladium is not incorporated into perovskite structure and remains as separate phase, which is reduced to Pd-0 at 1200 degrees C. X-ray photoelectron spectroscopy (XPS) reveled the presence of Pd2+, which indicate a reoxidation of Pd-0 in the surface layers during cooling. The Pd content in the samples has a small influence on the methane oxidation activity below the temperature of 500 degrees C. At temperatures higher than 500 C, the methane oxidation activity of the sample with x = 0.05 exceeds the activity of the sample with x = 0.10. The sharp increase of methane oxidation activity over the sample with lower content of palladium at about 500 degrees C was ascribed to the higher dispersion of PdO and Pd-0 phases. Thus, the higher contribution of lattice oxygen and possible local change in oxidation state of palladium can be a reason for the enhanced activity. Contrary to the supported Pd/Al2O3 catalyst, the incorporation of palladium into perovskite matrix and interaction of PdO-Pd-0 benefits the activity of smaller particles at higher reaction temperatures.
PB  - Elsevier Science Bv, Amsterdam
T2  - Applied Catalysis B: Environmental
T1  - Catalytic combustion of methane over Pd containing perovskite type oxides
SP  - 133
EP  - 141
VL  - 58
IS  - 1-2
DO  - 10.1016/j.apcatb.2004.11.020
UR  - https://hdl.handle.net/21.15107/rcub_dais_4838
ER  - 
@article{
author = "Petrović, Srđan and Karanović, Ljiljana and Stefanov, Plamen K. and Zdujić, Miodrag and Terlecki Baričević, Ana",
year = "2005",
abstract = "The mixed perovskite type oxides with nominal formula LaTi0.5Mg0.5-xPdxO3, (0  LT = x  LT = 0.10) were prepared by anneling the ethanol solution of precursor in nitrogen flow at 1200 degrees C. X-ray powder diffraction (XRPD) analysis shows that the orthorhombic perovskite structure was found in all investigated samples. However, at least a part of palladium is not incorporated into perovskite structure and remains as separate phase, which is reduced to Pd-0 at 1200 degrees C. X-ray photoelectron spectroscopy (XPS) reveled the presence of Pd2+, which indicate a reoxidation of Pd-0 in the surface layers during cooling. The Pd content in the samples has a small influence on the methane oxidation activity below the temperature of 500 degrees C. At temperatures higher than 500 C, the methane oxidation activity of the sample with x = 0.05 exceeds the activity of the sample with x = 0.10. The sharp increase of methane oxidation activity over the sample with lower content of palladium at about 500 degrees C was ascribed to the higher dispersion of PdO and Pd-0 phases. Thus, the higher contribution of lattice oxygen and possible local change in oxidation state of palladium can be a reason for the enhanced activity. Contrary to the supported Pd/Al2O3 catalyst, the incorporation of palladium into perovskite matrix and interaction of PdO-Pd-0 benefits the activity of smaller particles at higher reaction temperatures.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Applied Catalysis B: Environmental",
title = "Catalytic combustion of methane over Pd containing perovskite type oxides",
pages = "133-141",
volume = "58",
number = "1-2",
doi = "10.1016/j.apcatb.2004.11.020",
url = "https://hdl.handle.net/21.15107/rcub_dais_4838"
}
Petrović, S., Karanović, L., Stefanov, P. K., Zdujić, M.,& Terlecki Baričević, A.. (2005). Catalytic combustion of methane over Pd containing perovskite type oxides. in Applied Catalysis B: Environmental
Elsevier Science Bv, Amsterdam., 58(1-2), 133-141.
https://doi.org/10.1016/j.apcatb.2004.11.020
https://hdl.handle.net/21.15107/rcub_dais_4838
Petrović S, Karanović L, Stefanov PK, Zdujić M, Terlecki Baričević A. Catalytic combustion of methane over Pd containing perovskite type oxides. in Applied Catalysis B: Environmental. 2005;58(1-2):133-141.
doi:10.1016/j.apcatb.2004.11.020
https://hdl.handle.net/21.15107/rcub_dais_4838 .
Petrović, Srđan, Karanović, Ljiljana, Stefanov, Plamen K., Zdujić, Miodrag, Terlecki Baričević, Ana, "Catalytic combustion of methane over Pd containing perovskite type oxides" in Applied Catalysis B: Environmental, 58, no. 1-2 (2005):133-141,
https://doi.org/10.1016/j.apcatb.2004.11.020 .,
https://hdl.handle.net/21.15107/rcub_dais_4838 .
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