Ariela Burg

Dr. Ariela Burg

Sami Shamoon College of Engineering, Chemical Engineering Department, Israel

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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3 September 2014 in Chemical Communications
Verified
Journal Article
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Ariela BurgAriela Burg
Ariela Burg
DSDror Shamir
Dror Shamir
ISInna Shusterman
Inna Shusterman
HKHaya Kornweitz
Haya Kornweitz
Dan - MeyersteinDan - Meyerstein
Dan - Meyerstein
The reaction Co(H 2 O) 6 2+ + H 2 O 2 proceeds via a transient that decomposes into Co II (H 2 O)(OOH)(OH) 2 + CO 3 ˙ − . Plausible biological implications are pointed out.

8 May 2014 in Dalton Transactions
Verified
Journal Article
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Ariela BurgAriela Burg
Ariela Burg
ISInna Shusterman
Inna Shusterman
HKHaya Kornweitz
Haya Kornweitz
Dan - MeyersteinDan - Meyerstein
Dan - Meyerstein
Co(II) complexes and Co(H2O)6 2+ are used as catalysts in advanced oxidation processes. Therefore it was decided to study the kinetics of reaction of Co(H2O)6 2+ with H2O2. Surprisingly, the kinetic results point out that the process involves three consecutive reactions, each of them requiring an H2O2 molecule, i.e. three H2O2 molecules ligate to the central cobalt cation prior to the formation of radicals. DFT analysis suggests that the transient (H2O)3CoII(OOH)2(H2O2) decomposes via: (H2O)3CoII(OOH)2(H2O2) → (H2O)3CoII(OOH)(˙OOH)(OH) + ˙OH ΔG0 = −5.975 kcal mol−1, with no evidence for the formation of a Co(III) transient. It is proposed that analogous mechanisms are involved whenever the redox potential of the central cation is too high to enable the reaction: M(H2O)6 n+ + H2O2 → M(n+1)+ aq + ˙OH + OH−.

19 July 2017 in Dalton Transactions
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Journal Article
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Ariela BurgAriela Burg
Ariela Burg
WYWolfer Yaniv
Wolfer Yaniv
SDShamir Dror
Shamir Dror
KHKornweitz Haya
Kornweitz Haya
AYAlbo Yael
Albo Yael
Dan - MeyersteinDan - Meyerstein
Dan - Meyerstein
NiL i 2+ are good electro-catalysts for water oxidation in phosphate/carbonate buffers. The active species are L(X)Ni IV OH 4−(3−n+1)/(2−n+1) . Carbonate behaves differently from phosphate.

20 October 2015 in Marine Drugs
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Journal Article
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Ariela BurgAriela Burg
Ariela Burg
Oshrat Levy-OntmanOshrat Levy-Ontman
Oshrat Levy-Ontman
Sulfated polysaccharides produced by microalgae, which are known to exhibit various biological activities, may potentially serve as natural antioxidant sources. To date, only a few studies have examined the antioxidant bioactivity of red microalgal polysaccharides. In this research, the effect of different salts on the antioxidant activities of two red microalgal sulfated polysaccharides derived from Porphyridium sp. and Porphyridium aerugineum were studied in a soy bean-based infant milk formula. Salt composition and concentration were both shown to affect the polysaccharides’ antioxidant activity. It can be postulated that the salt ions intefer with the polysaccharide chains’ interactions and alter their structure, leading to a new three-dimensional structure that better exposes antiooxidant sites in comparison to the polysaccharide without salt supplement. Among the cations that were studied, Ca2+ had the strongest enhancement effect on antioxidant activities of both polysaccharides. Understanding the effect of salts on polysaccharides’ stucture, in addition to furthering knowledge on polysaccharide bioactivities, may also shed light on the position of the antioxidant active sites.

1 January 2022 in Chemosphere
Verified
Journal Article
Closed access
SSShira Biton Seror
Shira Biton Seror
DSDror Shamir
Dror Shamir
YAYael Albo
Yael Albo
HKHaya Kornweitz
Haya Kornweitz
Ariela BurgAriela Burg
Ariela Burg

26 June 2020 in Molecules
Verified
Journal Article
Open access
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ZSZorik Shamish
Zorik Shamish
Moshe ZoharMoshe Zohar
Moshe Zohar
DSDror Shamir
Dror Shamir
Ariela BurgAriela Burg
Ariela Burg
We use dip-pen nanolithography to accurately pattern Ni(OH)2 nanoclusters on a metachemical surface with an exceptionally large surface area. The distance between the nanoclusters can be manipulated to control the oxygen-evolution reaction current and overpotential, thereby improving the efficiency of the water-splitting process while using minute amounts of the catalyst.