Modification of nZVI with a bio-conjugate containing amine and carbonyl functional groups for catalytic activation of persulfate

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F46747885%3A24620%2F21%3A00007860" target="_blank" >RIV/46747885:24620/21:00007860 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61989592:15640/21:73607328

Výsledek na webu

<a href="https://www.sciencedirect.com/science/article/pii/S1383586620323534" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1383586620323534</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.seppur.2020.117880" target="_blank" >10.1016/j.seppur.2020.117880</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Modification of nZVI with a bio-conjugate containing amine and carbonyl functional groups for catalytic activation of persulfate

Popis výsledku v původním jazyce

Although the catalytic activation of persulfate by iron is now common in environmental sciences, there are still several obstacles, including the non-selectiveness and high cost of the production of the iron catalyst. Therefore, it is essential to develop fast and easy methods for producing an iron catalyst that exhibits high surface area properties and rapid catalytic activation of persulfate. In the present work, a chitosan-poly(3–hydroxybutyrate) conjugate (CS-PHB) was used to improve the synthesis of nanoscale zero-valent iron (nZVI). CS-PHB possesses among others two functional groups (carbonyl and amine) that are desirable for catalytic applications, including heterogeneous persulfate activation. The produced CS-PHB-nZVI particles showed an extensive surface area (113 m2/g) and, at the same time, superior activity in heterogeneous catalysis, which was tested and compared with others persulfate activation methods (heat, Fe2 , commercial nZVI). The most suitable activation conditions for complete degradation of 0.15 mM of the model pollutant (methyl orange; MO) were determined (i.e., a pH of 7, persulfate and CS-PHB-nZVI concentrations of 2 mM and 50 mg/L, respectively). The role of temperature in MO oxidation was evaluated by the Arrhenius equation, and the results showed that the estimated activation energy (Ea) was 27.1 kJ/mol. The MO degradation may be attributed to the generation of SO4radical dot− in the system as a result of scavenging tests. A magnet can be used to easily separate the remaining catalyst. It is believed that due to it having several advantages over traditionally used nZVI, CS-PHB-nZVI may be successfully applied for catalytic remediation of contaminants that are reactive towards sulfate radicals.

Název v anglickém jazyce

Modification of nZVI with a bio-conjugate containing amine and carbonyl functional groups for catalytic activation of persulfate

Popis výsledku anglicky

Although the catalytic activation of persulfate by iron is now common in environmental sciences, there are still several obstacles, including the non-selectiveness and high cost of the production of the iron catalyst. Therefore, it is essential to develop fast and easy methods for producing an iron catalyst that exhibits high surface area properties and rapid catalytic activation of persulfate. In the present work, a chitosan-poly(3–hydroxybutyrate) conjugate (CS-PHB) was used to improve the synthesis of nanoscale zero-valent iron (nZVI). CS-PHB possesses among others two functional groups (carbonyl and amine) that are desirable for catalytic applications, including heterogeneous persulfate activation. The produced CS-PHB-nZVI particles showed an extensive surface area (113 m2/g) and, at the same time, superior activity in heterogeneous catalysis, which was tested and compared with others persulfate activation methods (heat, Fe2 , commercial nZVI). The most suitable activation conditions for complete degradation of 0.15 mM of the model pollutant (methyl orange; MO) were determined (i.e., a pH of 7, persulfate and CS-PHB-nZVI concentrations of 2 mM and 50 mg/L, respectively). The role of temperature in MO oxidation was evaluated by the Arrhenius equation, and the results showed that the estimated activation energy (Ea) was 27.1 kJ/mol. The MO degradation may be attributed to the generation of SO4radical dot− in the system as a result of scavenging tests. A magnet can be used to easily separate the remaining catalyst. It is believed that due to it having several advantages over traditionally used nZVI, CS-PHB-nZVI may be successfully applied for catalytic remediation of contaminants that are reactive towards sulfate radicals.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

20402 - Chemical process engineering

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2021

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Separation and Purification Technology

ISSN

1383-5866

e-ISSN

—

Svazek periodika

257

Číslo periodika v rámci svazku

February

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

11

Strana od-do

—

Kód UT WoS článku

000596380900006

EID výsledku v databázi Scopus

2-s2.0-85092893268