Bartosz Środa

Mr. Bartosz Środa

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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5 August 2023 in Journal of Energy Chemistry
Verified
Journal Article
Closed access
ADAnna Dymerska
Anna Dymerska
BŚBartosz Środa
Bartosz Środa
KSKrzysztof Sielicki
Krzysztof Sielicki
GLGrzegorz Leniec
Grzegorz Leniec
BZBeata Zielińska
Beata Zielińska
EMEwa Mijowska
Ewa Mijowska

Verified
Journal Article
Open access
PDF file
SMSzymon Macieja
Szymon Macieja
BŚBartosz Środa
Bartosz Środa
BZBeata Zielińska
Beata Zielińska
Swarup RoySwarup Roy
Swarup Roy
ABArtur Bartkowiak
Artur Bartkowiak
Łukasz ŁopusiewiczŁukasz Łopusiewicz
Łukasz Łopusiewicz
Green synthesis of nanoparticles for use in food packaging or biomedical applications is attracting increasing interest. In this study, the effect of the degree of substitution (0.7, 0.9 and 1.2) of a carboxymethylcellulose polymer matrix on the synthesis and properties of silver nanoparticles using melanin as a reductant was investigated. For this purpose, the mechanical, UV–Vis barrier, crystallinity, morphology, antioxidant and antimicrobial properties of the films were determined, as well as the color and changes in chemical bonds. The degree of substitution effected noticeable changes in the color of the films (the L* parameter was 2.87 ± 0.76, 5.59 ± 1.30 and 13.45 ± 1.11 for CMC 0.7 + Ag, CMC 0.9 + Ag and CMC 1.2 + Ag samples, respectively), the UV–Vis barrier properties (the transmittance at 280 nm was 4.51 ± 0.58, 7.65 ± 0.84 and 7.98 ± 0.75 for CMC 0.7 + Ag, CMC 0.9 + Ag and CMC 1.2 + Ag, respectively) or the antimicrobial properties of the films (the higher the degree of substitution, the better the antimicrobial properties of the silver nanoparticle-modified films). The differences in the properties of films with silver nanoparticles synthesized in situ might be linked to the increasing dispersion of silver nanoparticles as the degree of CMC substitution increases. Potentially, such films could be used in food packaging or biomedical applications.

17 February 2023 in International Journal of Hydrogen Energy
Verified
Journal Article
Closed access
BŚBartosz Środa
Bartosz Środa
ADAnna G. Dymerska
Anna G. Dymerska
Beata ZielińskaBeata Zielińska
Beata Zielińska
EMEwa Mijowska
Ewa Mijowska

11 October 2023 in RSC Advances
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Journal Article
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BŚBartosz Środa
Bartosz Środa
ADAnna G. Dymerska
Anna G. Dymerska
PMPiotr Miądlicki
Piotr Miądlicki
AWAgnieszka Wróblewska
Agnieszka Wróblewska
Beata ZielińskaBeata Zielińska
Beata Zielińska
This study explores Ti3C2 MXene catalysts for the reaction of α-pinene isomerization to get highly valuable products such as camphene, limonene, and tricyclene.

30 September 2020 in Acta Scientiarum Polonorum Zootechnica
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Journal Article
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XSXymena Stachurska
Xymena Stachurska
BŚBartosz Środa
Bartosz Środa
KDKamila Dubrowska
Kamila Dubrowska
JJJoanna Jabłońska
Joanna Jabłońska
MRMarta Roszak
Marta Roszak
JKJolanta Kochel-Karakulska
Jolanta Kochel-Karakulska
The aim of this study was to isolate microorganisms with bioremediation potential from soil contaminated with heavy metal compounds, and to analyze the tolerance of these microorganisms to various heavy metal concentrations. In total, 7 bacterial strains were isolated and cultivated. The sensitivity of microorganisms to heavy metals proved to be dependent on the type of medium. The use of liquid media during the 8-hour and 24-hour toxicity tests resulted in reduced tolerance of isolates to the concentrations of selective factors used, relative to culture on solid substrates. In addition, optical density increases in the bacterial cultures have been observed at the highest concentrations of some heavy metals. Briefly, during the 48-hours test 3 strains showed increased optical density values in the presence of 1 mM copper sulfate and 2 strains displayed this ability also in the presence of 1 mM cadmium sulfate and lead nitrate.

1 January 2022 in SSRN Electronic Journal
Verified
Preprint
Open access
PDF file
ADAnna Dymerska
Anna Dymerska
BŚBartosz Środa
Bartosz Środa
Beata ZielińskaBeata Zielińska
Beata Zielińska
EMEwa Mijowska
Ewa Mijowska
Hydrogen is a promising energy source which can replace fossil fuels. Among the methods of generating hydrogen, electrochemical water splitting is distinguished by its high renewability efficiency, sustainability and ability to produce this element without the limitation of geological conditions and scaling devices. However, electrochemical water splitting is thermodynamically unfavourable, especially by its oxidation half-reaction (OER) and commercially available catalysts are expensive and have not-abundant natural resources. Therefore, the design of a new, cheap and easy-to-produce material for the efficient evolution of hydrogen from water splitting (HER) is required to accelerate the kinetics of the OER, reduce the energy requirements and improve the durability of its work. Various new technologies and active materials have recently been developed in electrochemical water splitting for hydrogen production. Among them, depending on the preparation method, chemical composition and the morphology of the electrocatalysts influencing the efficiency of both half-reactions of water splitting are still full of gaps of knowledge. Therefore, in this work, we demonstrate a smart methodology to selectively activate NiMOF-based active material in hydrogen and oxygen evolution reactions by designed electrode fabrication. We demonstrate high-performance electrocatalysts based on Nickel/metal-organic frameworks (NiMOF) fabricated via two routes: A - drop cast on pristine Nickel foam active in OER (flower-like structure), B - Ni foam in situ impregnated by NiMOF during synthesis active in HER (rectangular like structure). It allows for the demonstration of a series of highly efficient and robust electrocatalysts. Furthermore, in-situ studies on structural changes in the active materials have been conducted to reveal the mechanisms of water splitting half-reactions.