Mark Žic

Dr. Mark Žic

Ruđer Bošković Institute, P.O. Box 180, 10000 Zagreb, Croatia

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 August 2018 in Polymers
Verified
Journal Article
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VGVanja Gilja
Vanja Gilja
IVIvan Vrban
Ivan Vrban
VMVilko Mandić
Vilko Mandić
MŽMark Žic
Mark Žic
ZHZlata Hrnjak-Murgić
Zlata Hrnjak-Murgić
Polyaniline/zinc oxide (PANI/ZnO) composite photocatalysts were prepared from neutral media by in situ chemical oxidation of aniline (ANI) in the presence of different amounts of diethylene glycol (DEG). The PANI/ZnO composite photocatalysts were synthesized to efficiently remove organic dye (acid blue, AB25) from model wastewater. The PANI/ZnO composite photocatalysts were studied with the intention of efficient removal of organic dye (acid blue, AB25) from wastewater to obtain low-cost heterogeneous catalysts that offer high catalytic activity and stability. The conductive PANI polymer, which absorbs Vis irradiation, was used in this work as ZnO absorbs only ultraviolet (UV) irradiation; thus, the composite photocatalysts’ activity was broadened into the Vis region. Characterization of the composite photocatalysts was done by Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, scanning electron microscopy, electric conductivity, UV-Vis spectroscopy, and by specific surface area (SBET) measurements. The composites’ photocatalytic activity under solar irradiation was validated by monitoring degradation of the AB25 dye. This study presented that it was possible both to prepare PANI and to prevent ZnO dissolution if in situ polymerization starts from neutral media with the addition of DEG. Additionally, efficient removal of AB25 dye, about 90% in 60 min, was achieved. The first-order rate constants of the photodegradation of AB25 by PANI/ZnO 0.02/0.024/0.04 DEG (and pure ZnO)) were computed to be 0.0272/0.0281/0.0325 (and 0.0062) min−1, indicating that the morphology and surface of the photocatalysts have significantly influenced the catalytic activity.

23 November 2017 in Nanomaterials
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VGVanja Gilja
Vanja Gilja
KNKatarina Novaković
Katarina Novaković
JTJadranka Travas-Sejdic
Jadranka Travas-Sejdic
ZHZlata Hrnjak-Murgić
Zlata Hrnjak-Murgić
MRMarijana Kraljić Roković
Marijana Kraljić Roković
MŽMark Žic
Mark Žic
The polyaniline/TiO2 (PANI/TiO2) composite photocatalysts were prepared by the in situ chemical oxidation of aniline (An) in the presence of TiO2 particles. For this purpose, photocatalysts with different amounts of PANI polymer were prepared and analysed. Fourier-transform infrared (FT-IR) spectroscopy and thermogravimetric (TG) analysis indicated successful synthesis of the PANI polymer and its conductivity was also determined. The micrographs of field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) were used to explain the impact of the aniline amount on the aggregation process during the synthesis of the composites. The smallest size of aggregates was obtained for the photocatalysts with 15% of PANI (15PANI/TiO2) due to the formation of homogenous PANI. The photocatalytic activity of studied PANI/TiO2 photocatalysts was validated by monitoring the discoloration and mineralization of Reactive Red azo dye (RR45) in wastewater. The 15PANI/TiO2 sample presented the highest photocatalytic efficiency under ultraviolet A (UVA) irradiation, in comparison to pure TiO2. This was explained by the formation of uniformly dispersed PANI on the TiO2 particles, which was responsible for the synergistic PANI-TiO2 effect.

1 May 2007 in Journal of Molecular Structure
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Journal Article
Closed access
MŽMark Žic
Mark Žic
MRMira Ristić
Mira Ristić
SMSvetozar Musić
Svetozar Musić

30 November 2019 in GEM - International Journal on Geomathematics
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MŽMark Žic
Mark Žic
SPSergiy Pereverzyev
Sergiy Pereverzyev
VSVanja Subotić
Vanja Subotić
SPSergei Pereverzyev
Sergei Pereverzyev
Determination of the distribution function of relaxation times (DFRT) is an approach that gives us more detailed insight into system processes, which are not observable by simple electrochemical impedance spectroscopy (EIS) measurements. DFRT maps EIS data into a function containing the timescale characteristics of the system under consideration. The extraction of such characteristics from noisy EIS measurements can be described by Fredholm integral equation of the first kind that is known to be ill-posed and can be treated only with regularization techniques. Moreover, since only a finite number of EIS data may actually be obtained, the above-mentioned equation appears as after application of a collocation method that needs to be combined with the regularization. In the present study, we discuss how a regularized collocation of DFRT problem can be implemented such that all appearing quantities allow symbolic computations as sums of table integrals. The proposed implementation of the regularized collocation is treated as a multi-parameter regularization. Another contribution of the present work is the adjustment of the previously proposed multiple parameter choice strategy to the context of DFRT problem. The resulting strategy is based on the aggregation of all computed regularized approximants, and can be in principle used in synergy with other methods for solving DFRT problem. We also report the results from the experiments that apply the synthetic data showing that the proposed technique successfully reproduced known exact DFRT. The data obtained by our techniques is also compared to data obtained by well-known DFRT software (DRTtools).

1 September 2008 in Journal of Alloys and Compounds
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Journal Article
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MŽMark Žic
Mark Žic
MRMira Ristić
Mira Ristić
SMSvetozar Musić
Svetozar Musić

25 May 2021 in Materials
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MJMarko Jakovac
Marko Jakovac
TKTeodoro Klaser
Teodoro Klaser
BRBorna Radatovic
Borna Radatovic
ADArijeta Bafti Dunatov
Arijeta Bafti Dunatov
Željko SkokoŽeljko Skoko
Željko Skoko
MŽMark Žic
Mark Žic
Over the last decade, zirconia (ZrO2)-based ceramic materials have become more applicable to modern dental medicine due to the sustained development of diverse computer-aided design/computer-aided manufacturing (CAD/CAM) systems. However, before the cementation and clinical application, the freshly prepared zirconia material (e.g., crowns) has to be processed by sandblasting in the dental laboratory. In this work, the impact of the sandblasting on the zirconia is monitored as changes in morphology (i.e., grains and cracks), and the presence of impurities might result in a poor adhesive bonding with cement. The sandblasting is conducted by using Al2O3 powder (25, 50, 110 and 125 µm) under various amounts of air-abrasion pressure (0.1, 0.2, 0.4 and 0.6 MPa). There has been much interest in both the determination of the impact of the sandblasting on the zirconia phase transformations and conductivity. Morphology changes are observed by using Scanning Electron Microscope (SEM), the conductivity is measured by Impedance Spectroscopy (IS), and the phase transformation is observed by using Powder X-Ray Diffraction (PXRD). The results imply that even the application of the lowest amount of air-abrasion pressure and the smallest Al2O3 powder size yields a morphology change, a phase transformation and a material contamination.